CN106590852A - Industrial lubricating oil composition and production method therefor - Google Patents
Industrial lubricating oil composition and production method therefor Download PDFInfo
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- CN106590852A CN106590852A CN201510676771.7A CN201510676771A CN106590852A CN 106590852 A CN106590852 A CN 106590852A CN 201510676771 A CN201510676771 A CN 201510676771A CN 106590852 A CN106590852 A CN 106590852A
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- 0 CCC1N(*)C(CC)C(CC)SC1CC Chemical compound CCC1N(*)C(CC)C(CC)SC1CC 0.000 description 4
- BUASNINWKGJCHE-UHFFFAOYSA-N CC(C)(C)c1c(C)c(SCNc(cc2)ccc2Nc2ccccc2)cc(C)c1 Chemical compound CC(C)(C)c1c(C)c(SCNc(cc2)ccc2Nc2ccccc2)cc(C)c1 BUASNINWKGJCHE-UHFFFAOYSA-N 0.000 description 1
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Abstract
The invention relates to an industrial lubricating oil composition. The industrial lubricating oil composition contains a screening phenolic compound, an extreme-pressure antiwear additive, a metal deactivator, an antirusting agent and a major volume of lubricating oil base oil; and the structure of the screening phenolic compound is represented by a formula (I) shown in the description, wherein all groups in the formula (I) are as defined in the description. The industrial lubricating oil composition disclosed by the invention can meet the increasingly severe requirements of current higher-specification products on oxidation resistance and further display excellent cleaning and dispersion properties, extreme pressure property, wear resistance, corrosion resistance and rust resistance.
Description
Technical field
The present invention relates to a kind of industrial lubrication fluid composition.Specifically, the present invention relates to one
Plant long-life industrial lubrication fluid composition.
Background technology
Industrial lubricant is of wide application, including steam turbine oil, industrial gear oil, liquid
Force feed, Oil Film of Bearing Oil, turbine and worm oil, bobbin oil, antirust oil, rail oil, chain
Oil etc..
The combustion gas steam turbine that is widely used at present, steam steam turbine, waterpower steam turbine are required
Turbo-engine lube has higher bearing capacity and longer service life.Steam turbine
Lubricant housings be mainly gearbox and rotor bearing, because its rotor axle envelope is possible to alter vapour,
Therefore the possibility of the lubricating system water inlet is larger, in addition equipment rotating speed is high, load is big, fortune
Line period is long, therefore the requirement of the antioxygenic property, rust-preventing characteristic and resistance to emulsion to oil product is all very
It is high.Combustion gas steam turbine is directly done work using the combustion gas that burning is produced, combustion gas turbo-engine lube
By bearing hot surface effect and use under governing system high pressure, should have excellent oxidation
Stability and heat endurance, good antirust and demulsification performance.Steam-gas Combined is followed
Turbo-engine lube used by loop systems, then should meet steam turbine lubricating requirement, also
Meet the lubrication use requirement of combustion gas steam turbine.
Under industrial gear oil's harsh operating conditions usually in high temperature and high load capacity, table is needed
Reveal the performances such as good extreme pressure property, wear resistence, anti-oxidant and emulsion resistance.
With increasingly strict, other classes of technological progress and the environmental requirement of associated machines
The industrial lubricant of type is also at more harsh severe working environment.Therefore, in different journeys
Require that these industrial lubricants have longer service life, excellent load-carrying properties on degree
With abrasion resistance, excellent corrosion resistance and rustless property and good demulsification performance
Etc..
Seek the industrial lubricant of more efficiently antioxidant additive and exploitation novel high-performance,
The target that always those skilled in the art make great efforts.
United States Patent (USP) US 5304314 is disclosed and a kind of is suitable as the sulfur-bearing that antioxidant is used
With the phenolic compounds of arylamine.United States Patent (USP) US 2006/0189824A1 discloses a kind of being adapted to
As the shielding phenolic compounds containing secondary aromatic amine that antioxidant is used.
But, the compound of these prior arts when used in industrial lubricant, oil product
Still there is room for improvement in high-temperature oxidation resistance, extreme pressure bearing capacity and abrasion resistance.
In addition, in addition to the adverse effect of deposit, corrosion and corrosion also can serious curtailment metals
The performance of operating condition of part.Concern of the prior art to rustless property is also far from enough.
The content of the invention
The present invention relates to the content of following aspect.
1. a kind of industrial lubrication fluid composition, including shielding phenolic compounds, extreme pressure anti-wear additives,
Metal deactivator, antirust agent and major amount of lube base oil;
It is described shielding phenolic compounds structure be:
In logical formula (I), each group R is same to each other or different to each other, be each independently selected from hydrogen,
C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight
Mn is polyolefin-based for 300-3000), the group shown in logical formula (II) and logical formula (III)
Shown group, on condition that at least one group R is the group shown in logical formula (II);Respectively
Group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight or branched alkane
Base (is preferably each independently selected from hydrogen and C1-4Straight or branched alkyl),
In aforementioned each logical formula (II), (III) and (IV), each group L is mutually the same or not
Together, it is independently of one another groupWherein group R " is selected from hydrogen, C1-20Hydrocarbon
Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, preferably
Selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl;Each group
R2It is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl,
The group shown in group and logical formula (V) shown in logical formula (IV) is (preferably independently of one another
Selected from hydrogen, C1-10Group shown in straight or branched alkyl and logical formula (IV));Each group
RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20Straight or branched alkyl is (excellent
Choosing is each independently selected from hydrogen and C1-10Straight or branched alkyl);Each group RcPhase each other
It is same or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Straight chain
Or branched alkyl epoxide (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and
C1-10Straight or branched alkyl epoxide, is more preferably in cyclic groupUpper nitrogen-atoms
Contraposition);Y is 0 to 3 integer (preferably 0 or 1);Z be 0 to 3 integer it is (excellent
Select 0 or 1);N is 1 to 8 integer (preferably 1 or 2);N' be 0 to 7 integer it is (excellent
0,1 or 2) is selected, on condition that n'+n≤8 (preferred n'+n=1 or n'+n=2);Each group Rd
It is same to each other or different to each other, is each independently selected from hydrogen and the group shown in logical formula (V) is (excellent
Select hydrogen);Each cyclic groupIt is same to each other or different to each other, is each independently selected from phenyl ring
With naphthalene nucleus (preferred phenyl ring), wherein two adjacent cyclic groupsOptionally lead to each other
Cross additional S atom and bridge the N atoms of the two rings and form phenthazine ring, and/or,
Two adjacent cyclic groupsEach other optionally by additional group
(wherein group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and
C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen and C1-10Straight or branched alkyl) and
Bridge the N atoms of the two rings and form 9,10- acridan rings,
In logical formula (V), each group R is same to each other or different to each other, be each independently selected from hydrogen,
C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight
Mn is the polyolefin-based of 300-3000), the group shown in logical formula (II) and logical formula (III) institute
The group for showing (is preferably each independently selected from hydrogen and C1-300Straight or branched alkyl);Each base
Group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight or branched alkyl
(preferably it is each independently selected from hydrogen and C1-4Straight or branched alkyl);Group L is groupWherein group R " is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight chain is propped up
Alkyl group) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain is propped up
Alkyl group and C3-10Straight or branched miscellaneous alkyl;A be 0 or 1, and two group R and
One group-(S)a- L- occupies respectively three positions of residue on phenyl ring,
Wherein, the straight or branched miscellaneous alkyl is in straight or branched alkyl molecular structure
One or more (such as 1 to 4,1 to 3,1 to 2 or 1) in portion
Group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight or branched alkyl)
One of the substituting group group that directly substitutes and obtain and straight or branched alkyl molecule
One or more (such as 1 to 3,1 to 2 or 1) bases of inside configuration
Group-CH<By substituting group-N<The group for directly substituting and obtaining, wherein the shielding phenolate
Compound at least one group R in its whole molecular structuredIt is hydrogen.
2. according to the shielding phenolic compounds described in any preceding aspect, selected from following tool
The mixture of body compound or its arbitrary proportion:
3. a kind of industrial lubrication fluid composition, including shielding phenolic compounds, extreme pressure anti-wear additives,
Metal deactivator, antirust agent and major amount of lube base oil, the shielding phenolate is closed
The manufacture method of thing includes making shown in the phenolic compounds and formula (Y) shown in logical formula (X)
Amines in the presence of the aldehyde compound (preferred formaldehyde) shown in formula (Z) send out
The first step of raw reaction, optionally also includes making product and the sulfuration of the first step
Agent (preferred sulphur) react and/or with the aldehyde compound (preferred formaldehyde) shown in formula (Z)
The additional step of reaction,
In logical formula (X), each group R0It is same to each other or different to each other, is each independently selected from
Hydrogen ,-SH and C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or
Number-average molecular weight Mn is polyolefin-based for 300-3000's), on condition that at least one group R0
It is-SH;Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight chain
Or branched alkyl (is preferably each independently selected from hydrogen and C1-4Straight or branched alkyl),
In formula (Y), group R'2Selected from hydrogen, C1-20Straight or branched alkyl and groupEach group RbIt is same to each other or different to each other, is each independently selected from hydrogen
And C1-20Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-10Straight chain is propped up
Alkyl group);Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20
Straight or branched alkyl and C1-20Straight or branched alkyl epoxide (is preferably selected independently of one another
From hydrogen, C1-10Straight or branched alkyl and C1-10Straight or branched alkyl epoxide, more preferably
In cyclic groupThe contraposition of upper nitrogen-atoms);Y be 0 to 3 integer (preferably
0 or 1);Z is 0 to 3 integer (preferably 0 or 1);N1 be 1 to 8 integer it is (excellent
Select 1 or 2);Each cyclic groupIt is same to each other or different to each other, is each independently selected from
Phenyl ring and naphthalene nucleus (preferred phenyl ring),
In formula (Z), group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight chain or
Branched alkyl) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain or
Branched alkyl and C3-10Straight or branched miscellaneous alkyl,
Wherein, the straight or branched miscellaneous alkyl is in straight or branched alkyl molecular structure
One or more (such as 1 to 4,1 to 3,1 to 2 or 1) in portion
Group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight or branched alkyl)
One of the substituting group group that directly substitutes and obtain and straight or branched alkyl molecule
One or more (such as 1 to 3,1 to 2 or 1) bases of inside configuration
Group-CH<By substituting group-N<The group for directly substituting and obtaining.
4. according to the manufacture method described in any preceding aspect, wherein in the first step
In, the phenolic compounds shown in the logical formula (X) and the amination shown in the formula (Y)
The mol ratio of compound is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, it is described
Phenolic compounds shown in logical formula (X) rubs with the aldehyde compound shown in the formula (Z)
You are than being 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, in the extra step
In rapid, the amines shown in the formula (Y) is with the mol ratio of the vulcanizing agent
1:1-10, preferably 1:1.2-6.0, more preferably 1:1.5-3.0, the amine shown in the formula (Y)
Compound is 1 with the mol ratio of the aldehyde compound shown in the formula (Z):0.1-10, it is excellent
Select 1:0.5-5.0, more preferably 1:0.8-2.0.
5. in the industrial lubrication fluid composition described in any preceding aspect, the shielding phenol
Compound accounts for the 0.001%-30% of the industrial lubricant composition total weight, preferably
0.05%-20%, more preferably 0.1%-10%;
The extreme pressure anti-wear additives can be selected from olefine sulfide, phosphate derivative, D2EHDTPA
In ester derivant, dialkyl dithiocarbamate and dialkyl dithiophosphate one
Plant or various.The olefine sulfide can be selected from Shenyang extensively up to the sulphur of Chemical Co., Ltd.'s production
Change isobutene T321A, T321B and T321C, the sulfuration of Shandong east chemical fertilizer factory production is different
Butylene T321, the Anglamol33 of Lubrizol Corp. of the U.S., american exxon-XOM
Mobilad C-170 etc..The phosphate derivative can selected from di-n-butyl phosphite,
Phosphorous acid di-n-octyl, phosphorous acid diisobutyl ester, phosphorous acid di-isooctyl, tricresol phosphate
One or more in ester and phosphate amine salt, such as can be from Shandong Zibo favour China chemical industry
T304, T306, T308 and T308B of Co., Ltd's production, BASF Corp. of Germany's life
Irgalube353 of product etc..The phosphorothioate derivative can selected from thiophosphate,
The multiple ester amine salt of thiophosphate nitrogen containing derivative, thiophosphate, thiophosphate amine salt and
One or more in boronation thiophosphate amine salt, such as can select Jiangsu Danyang Bo Er
The T305 of petroleum additive Co., Ltd production, the life of Shandong Zibo Hui Hua Chemical Co., Ltd.
T307 of product, the SN3012 of Tianjin Shun Neng Chemical Companies production etc..The dioxane
Base dithiocar-bamate can selected from zinc dialkyl dithiocarbamate salt, lead salt and
One or more of antimonic salt, alkyl therein is the alkyl containing 2 to 12 carbon atoms,
Can be ethyl, n-propyl, different preferably containing the alkyl of 2 to 8 carbon atoms
Propyl group, normal-butyl, isobutyl group, sec-butyl, n-pentyl, isopentyl, n-hexyl, dissident
One or more in base, n-octyl, 2- ethylhexyls, cyclohexyl, methylcyclopentyl.
The dialkyl dithiophosphate can be selected from C2-12Alkyl ZDDP, is preferably selected from C3-8
Alkyl ZDDP, its alkyl can be from ethyl, n-propyl, isopropyl, normal-butyl, different
Butyl, sec-butyl, n-pentyl, isopentyl, n-hexyl, isohesyl, n-octyl, 2-
One or more in ethylhexyl, cyclohexyl and methylcyclopentyl.
The extreme pressure anti-wear additives are preferably selected from the group of olefine sulfide and phosphorothioate derivative
Close, the mass ratio in the combination between the two is 0.01:1-100:1, it is preferably in a proportion of 0.05:
1-20:1, more preferably ratio is 0.1:1-10:1.The extreme pressure anti-wear additives account for the work
The 0.01%-10% of industry lubricant oil composite gross mass, preferred 0.05%-8%, more preferably
0.1%-5%.
The metal deactivator can be selected from benzotriazole derivative and/or thiadiazoles derivative.
The benzotriazole derivative can selected from 1,2,3- BTAs, methyl benzotriazazole,
One kind in benzotriazole diakylaminomethylene derivative and benzotriazole fatty amine salt or
Various, alkyl therein is the alkyl containing 2 to 20 carbon atoms, is preferably contained
There is the alkyl of 2 to 8 carbon atoms, fatty amine is C2-20Kiber alkyl amine, preferred C6-18
Kiber alkyl amine, such as can from Shandong Zibo Hui Hua Chemical Co., Ltd. production T406,
T706 and T551, the T551B of Shandong Chengwu hot Chemical Co., Ltd. production, German bar
Reoment 38 of Si Fu-Ciba companies production etc..The thiadiazoles derivative can be selected from
2,5- dimercapto-1,3,4-thiadiazoles and/or 2,5- bis- (alkyl two is thio) thiadiazoles, wherein
Alkyl be the alkyl containing 2 to 20 carbon atoms, preferably containing 6 to 12
The alkyl of carbon atom, such as can be produced from Shandong Yantai Heng Nuo Chemical Industry Science Co., Ltd
DMTD, Shandong Chengwu hot Chemical Co., Ltd. production T561, the U.S.
Cuvan 484 of Vanderbilt companies production etc..
The metal deactivator is preferably selected from thiadiazoles derivative.The metal deactivator accounts for institute
The 0.01%-1% of industrial lubrication fluid composition gross mass, preferred 0.02%-0.5% are stated, it is more excellent
Select 0.03%-0.3%.
The antirust agent can be selected from sulfonate, alkyl imidazolidine derivatives and alkenyl succinic acid
One or more in derivative.The sulfonate can be selected from petroleum sodium sulfonate, oil sulphur
One or more in sour barium, dinonyl barium sulfonate and synthesis sulfonic acid magnesium, such as can select
The T701 of jiangsu wuxi Yu Lian lube oil additives Co., Ltd, Guangzhou gloomyization chemical industry is limited
Company production T702, Shanghai Mead jar (unit of capacitance) moral Chemical Co., Ltd. production T705, on
T707 of Hai Bo great Chemical Co., Ltd.s production etc..The alkyl imidazolidine derivatives can be with
Selected from alkyl imidazoline alkenyl succinate and/or alkyl phosphoric acid imidazoline salt, such as can be with
T703 from the production of Shanghai Mead jar (unit of capacitance) moral Chemical Co., Ltd. etc..The allyl butyrate two
Acid derivative can be selected from alkenyl succinic acid, alkenyl succinic acid ester and alkenyl imidazoline allyl butyrate
One or more in diacid salt, for example, can select dodecenylsuccinic acid, laurylene base
One or more in succinate and heptadecenyl imidazolidene succinate, commodity board
Number include T746 and T747 etc. of the production of Shanghai Mead jar (unit of capacitance) moral Chemical Co., Ltd..
The antirust agent is preferably selected from alkyl imidazoline alkenyl succinate and/or allyl butyrate two
Acid.The antirust agent accounts for the 0.001%-10% of the industrial lubrication fluid composition gross mass,
It is preferred that 0.005%-5%, more preferably 0.01%-1%.
The lube base oil, can be moistened from API I, II, III, IV and V class
One or more in lubricant base oil, such as can be selected from mineral lubricating oil and synthesis profit
One or more in lubricating oil, in preferred II, III and IV class lubricating oil base oil
Plant or various, most preferably IV class lubricating oils base oil.
The present invention industrial lubrication fluid composition in can also add antioxidant, detersive,
Dispersant, pour-point depressant, viscosity index improver, friction improver, anti emulsifier and anti-
One or more in infusion other lube oil additives.These additives can individually make
With, it is also possible to combination of two or more is used, and its consumption is used from the routine of this area
Amount, is not particularly limited.
6. the manufacture method of the industrial lubrication fluid composition of any preceding aspect, including making
The shielding phenol, extreme pressure anti-wear additives, metal deactivator, antirust agent and the lubrication oil base
The step of plinth oil mixing.
Technique effect
Shielding phenolic compounds of the invention, phosphorus element-containing and metallic element, are not difficult to produce
Raw ash content, is environmentally friendly antioxidant.
Shielding phenolic compounds of the invention, the compound phase ratio with prior art shows
Go out the high-temperature oxidation resistance (heat endurance) for significantly improving, can effectively improve such as
(high temperature) oxidation stability of lubricating oil.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing
While excellent high-temperature oxidation resistance, excellent rustless property is also exhibited further.
This is not available for prior art compound.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing
While excellent high-temperature oxidation resistance, excellent cleansing performance is also exhibited further
(i.e. deposit generation rejection).This is not available for prior art compound.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing
While excellent high-temperature oxidation resistance, also exhibit further excellent extreme pressure property and
Abrasion resistance.This is not available for prior art compound.
The present invention industrial lubrication fluid composition show excellent antioxygenic property, peace and quiet point
Scattered performance, extreme pressure property, abrasion resistance, corrosion resistance and rustless property, fully meet
The requirement of middle load and heavy-duty industry lube product.
Specific embodiment
The specific embodiment of the present invention is described in detail below, however it is necessary that point out
It is that protection scope of the present invention is not limited to these specific embodiments, but by attached
Claims of record are determining.
All publications, patent application, patent and other bibliography that this specification is mentioned
All draw in this for reference.Unless otherwise defined, all technologies used by this specification and section
Technics all has the implication that those skilled in the art routinely understand.In case of conflict,
It is defined by the definition of this specification.
When this specification is with prefix " as well known to those skilled in the art ", " prior art " or its class
When coming derived materials, material, method, step, device or part etc. like term, the prefix
Derived object covers those commonly used in the art when the application is proposed, but also includes mesh
It is front to be also of little use, but by become it is art-recognized be suitable for be similar to purpose those.
In the context of the present specification, in addition to the content for clearly stating, do not mention
Any matters or item directly be suitable for it is known in the art those and any changing need not be carried out
Become.And, any embodiment described herein can be a kind of or many with described herein
Plant other embodiment freely to combine, the technical scheme or technological thought for being formed therefrom is regarded
For original disclosure of the invention or a part for original description, and it is not considered as herein not
The new content for disclosing or being expected, unless those skilled in the art think that the combination is substantially not
Reasonably.
In the context of the present invention, state " halogen " and refer to fluorine, chlorine, bromine or iodine.
In the context of the present invention, term " alkyl " has conventionally known in the art
Implication, including straight or branched alkyl, straight or branched thiazolinyl, straight or branched alkynyl,
Cycloalkyl, cycloalkenyl group, cycloalkynyl radical, aryl or its combination group, wherein it is preferred that straight chain or
Alkyl group, straight or branched thiazolinyl, aryl or its combination group.As the alkyl, tool
Body can such as enumerate C1-20Alkyl, including C1-20Straight or branched alkyl, C2-20Straight chain
Or branched-chain alkenyl, C2-20Straight or branched alkynyl, C3-20Cycloalkyl, C3-20Cycloalkenyl group,
C3-20Cycloalkynyl radical, C6-20Aryl or its combination group, wherein it is preferred that C1-20Straight or branched
Alkyl, C6-20Aryl or its combination group.As the combination group, such as can be with
Enumerate one or more C1-20Straight or branched alkyl (preferably one or more C1-10Directly
Chain or branched alkyl) and one or more C6-20Aryl (preferred one or more phenyl
Or naphthyl) group that obtained by Direct Bonding.As the combination group, such as
One or more C can further be enumerated1-10Straight or branched alkyl phenyl, phenyl C1-10Directly
Chain or branched alkyl or one or more C1-10Straight or branched alkyl phenyl C1-10Straight chain is propped up
Alkyl group etc., wherein more preferably C1-10
Straight or branched alkyl phenyl (such as tert-butyl-phenyl), phenyl C1-10Straight chain or
Branched alkyl (such as benzyl) or C1-10Straight or branched alkyl phenyl C1-10Straight chain
Or branched alkyl (such as t-butylbenzyl).
In the context of the present invention, so-called " straight or branched miscellaneous alkyl ", refers to straight chain
Or branched alkyl molecular structure inside is not (including main chain or any side in the alkyl molecule structure
The end of chain) one or more (such as 1 to 4,1 to 3,1 to 2 or
Person 1) group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight chain or
Branched alkyl) one of the substituting group group that directly substitutes and obtain or straight chain or
Branched alkyl molecular structure inside is not (including main chain or any side chain in the alkyl molecule structure
End) one or more (such as 1 to 3,1 to 2 or 1) bases
Group-CH<By substituting group-N<The group for directly substituting and obtaining.As the replacement base
Group, preferably-O- or-S-, more preferably-S-.It is apparent that from the angle of structural stability
For, when having multiple, not Direct Bonding between these substituting groups.In addition,
Although the carbon number of the straight or branched alkyl is because group-CH2- or group-CH<Quilt
Substitute and accordingly reduce, but in order to state simplicity, still with the replacement as described before straight chain or
The carbon number of branched alkyl refers to the carbon number of the straight or branched miscellaneous alkyl.As
The straight or branched miscellaneous alkyl, for concrete example, C4Straight chained alkyl is such as(group in formula indicated by arrow is not in molecule
Inside configuration, but in the end of main chain) by a substituting group-O- directly substitute by
Obtain --- CH2-O——CH2-CH3Or --- CH2-CH2-O——CH3,
Referred to as C4Linear heteroalkyl group.Or, C4Branched alkyl is such as(group in formula indicated by arrow is not in molecular structure
Portion, but in main chain and the end of side chain) by a substituting group-N<Directly substituting will
ObtainReferred to as C4Branched heteroalkyl groups.According to the present invention,
As the straight or branched miscellaneous alkyl, such as can enumerate C3-20The miscellaneous alkane of straight or branched
Base, wherein it is preferred that C3-10Straight or branched miscellaneous alkyl or C3-6Straight or branched miscellaneous alkyl.
In the context of the present specification, expression way " numeral+valency+group " or it is similar
Term is referred to from the foundation structure (such as chain, ring or its combination etc.) corresponding to the group
It is upper remove the numeral representated by quantity hydrogen atom after obtain group, preferably refer to from
On carbon atom (preferred saturated carbon atom and/or non-same carbon atom) contained by the structure
The group obtained after the hydrogen atom for removing the quantity representated by the numeral.For example, " 3
Valency straight or branched alkyl " is referred to from straight or branched alkane (i.e. straight or branched alkane
Basic chain corresponding to base) on remove 3 hydrogen atoms and the group that obtains, and " divalent is straight
Chain or branched heteroalkyl groups " are then referred to from the miscellaneous alkane of straight or branched (preferably from the miscellaneous alkane
Contained carbon atom, or further, from non-same carbon atom) on remove 2 hydrogen
Atom and the group that obtains.
In the case where not clearly indicating, all percentages for being previously mentioned in this specification,
Number, ratio etc. are all on the basis of weight, unless do not met this when on the basis of weight
The conventional understanding of art personnel.
In the context of the present specification, in case of no particular description, the equal molecule of number
Amount Mn is determined by gel permeation chromatography (GPC).
In the context of the present specification, in case of no particular description, it is any to be related to
Gel permeation chromatography (GPC) or the condition determination of GPC spectrograms be:Instrument:The U.S.
Waters companies waters2695 type gel osmoticing chromatogram analysis instrument;Mobile phase adopts tetrahydrochysene furan
Mutter, flow velocity is 1mL/min, chromatogram column temperature is 35 DEG C, delivery time 40min, sample
Mass fraction is 0.16%-0.20%.
According to the present invention, the shielding phenolic compounds being related to shown in a kind of logical formula (I).
According to the present invention, in logical formula (I), when having multiple, each group R is each other
It is identical or different, it is each independently selected from hydrogen, C1-300Straight or branched alkyl, logical formula (II)
Group shown in shown group and logical formula (III), on condition that at least one group R is
Group shown in logical formula (II).
According to the present invention, in logical formula (I), as the C1-300Straight or branched alkyl,
C can such as be enumerated1-20Straight or branched alkyl (preferred C1-10Straight or branched alkyl,
More preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As described polyolefin-based,
It is concrete such as to enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000.Now,
As polyolefin-based number-average molecular weight Mn, preferred 500-2000, more preferably
500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is presented
For chain alkyl structure), but depending on the polyolefinic species as initiation material or this is poly-
It is likely to containing a small amount of alkene in the difference of alkene manufacture method, the polyolefin-based strand
Category double bond (is remained such as in polyolefin manufacturing process or introduced), but this has no effect on
The realization of effect of the present invention, the present invention also has no intention to carry out clearly the amount, and the present invention
Still polyolefin-based classify as this " alkyl ".
, in logical formula (I), there are multiple group R in an embodiment of the invention,
One of group R is to lead to the group shown in formula (II), in two other group R
It is individual be it is described polyolefin-based, another is hydrogen, C1-20Straight or branched alkyl (preferred C1-10
Straight or branched alkyl) or logical formula (III) shown in group.
An embodiment of the invention, in logical formula (I), when group R is institute
When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (I).
According to the present invention, in logical formula (I), when having multiple, each group R' is each other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (I), when having multiple,
Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane
Base.
According to the present invention, in logical formula (II), group L is
According to the present invention, in logical formula (II), in the definition of group L, group R "
Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up
Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (II), in determining for group L
In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous
Alkyl.
According to the present invention, in logical formula (II), group R2Selected from hydrogen, C1-20Straight chain is propped up
Group and the group shown in logical formula (V) shown in alkyl group, logical formula (IV).
An embodiment of the invention, in logical formula (II), group R2Selected from hydrogen,
C1-10Group shown in straight or branched alkyl and logical formula (IV).
According to the present invention, in logical formula (II), when having multiple, each group RbEach other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl, it is preferably each
From independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (II), when having multiple,
Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched
Alkyl, preferred hydrogen.
According to the present invention, in logical formula (II), when having multiple, each group RcEach other
It is identical or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly
Chain or branched alkyl epoxide.
An embodiment of the invention, in logical formula (II), when having multiple,
Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched
Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (II), preferably one group
RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding)
Contraposition.
According to the present invention, in logical formula (II), y is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in logical formula (II), z is 0 to 3 integer, preferably 0 or 1.
According to the present invention, in logical formula (II), n is 1 to 8 integer, preferably 1 or
2。
According to the present invention, in logical formula (II), when having multiple, each group RdEach other
It is identical or different, it is each independently selected from hydrogen and the group shown in logical formula (V), preferred hydrogen.
According to the present invention, in logical formula (II), when having multiple, each cyclic group
(being rendered as divalent group in the inside configuration of logical formula (II)) is same to each other or different to each other, respectively
From independently selected from phenyl ring, (inside configuration preferably in logical formula (II) is rendered as 1,4- Asias benzene
Base) and naphthalene nucleus (inside configuration preferably in logical formula (II) is rendered as 1,4- or 2,6- Asias naphthalene
Base), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (II), two adjacent rings
GroupCan pass through each other additional S atom (not showing in structural formula) and
The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen
Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (II), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should
Phenthazine ring.
An embodiment of the invention, in logical formula (II), two adjacent rings
GroupAdditional group can be passed through each other(in structural formula not
Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding)
And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon
Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R "
Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (II), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups
GroupIn each with another adjacent cyclic groupFormed
The acridan ring.
According to the present invention, in logical formula (III), group L is
According to the present invention, in logical formula (III), in the definition of group L, group R "
Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up
Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (III), in determining for group L
In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous
Alkyl.
According to the present invention, in logical formula (III), group R2Selected from hydrogen, C1-20Straight chain or
Group and the group shown in logical formula (V) shown in branched alkyl, logical formula (IV).
An embodiment of the invention, in logical formula (III), group R2It is selected from
Hydrogen, C1-10Group shown in straight or branched alkyl and logical formula (IV).
According to the present invention, in logical formula (III), when having multiple, each group RbThat
This is identical or different, is each independently selected from hydrogen and C1-20Straight or branched alkyl, preferably
It is each independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (III), when having multiple,
Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched
Alkyl, preferred hydrogen.
According to the present invention, in logical formula (III), when having multiple, each group RcThat
This is identical or different, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20
Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (III), when having multiple,
Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched
Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (III), preferably one group
RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding)
Contraposition.
According to the present invention, in logical formula (III), y is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in logical formula (III), z is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in logical formula (III), n is 1 to 8 integer, preferably 1 or
2。
According to the present invention, in logical formula (III), when having multiple, each group RdThat
This is identical or different, is each independently selected from hydrogen and the group shown in logical formula (V), preferably
Hydrogen.
According to the present invention, in logical formula (III), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of logical formula (III)) is mutually the same
Or it is different, (inside configuration preferably in logical formula (III) is presented to be each independently selected from phenyl ring
For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in logical formula (III) is rendered as 1,4-
Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (III), two adjacent rings
GroupCan pass through each other additional S atom (not showing in structural formula) and
The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen
Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (III), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should
Phenthazine ring.
An embodiment of the invention, in logical formula (III), two adjacent rings
GroupAdditional group can be passed through each other(in structural formula not
Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding)
And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon
Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R "
Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (III), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups
GroupIn each with another adjacent cyclic groupFormed
The acridan ring.
According to the present invention, in logical formula (IV), when having multiple, each group RbThat
This is identical or different, is each independently selected from hydrogen and C1-20Straight or branched alkyl, preferably
It is each independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (IV), when having multiple,
Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched
Alkyl, preferred hydrogen.
According to the present invention, in logical formula (IV), when having multiple, each group RcThat
This is identical or different, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20
Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (IV), when having multiple,
Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched
Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (IV), preferably one group
RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding)
Contraposition.
According to the present invention, in logical formula (IV), y is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in logical formula (IV), z is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in logical formula (IV), n' is 0 to 7 integer, preferably 0,1
Or 2, on condition that n'+n≤8.An embodiment of the invention, n'+n=1 or n'+n=2.
Here, n is identical with the definition in aforementioned formula (II).
According to the present invention, in logical formula (IV), when having multiple, each group RdThat
This is identical or different, is each independently selected from hydrogen and the group shown in logical formula (V), preferably
Hydrogen.
According to the present invention, in logical formula (IV), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of logical formula (IV)) is mutually the same
Or it is different, (inside configuration preferably in logical formula (IV) is presented to be each independently selected from phenyl ring
For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in logical formula (II) is rendered as 1,4-
Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (IV), two adjacent rings
GroupCan pass through each other additional S atom (not showing in structural formula) and
The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen
Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (IV), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should
Phenthazine ring.
An embodiment of the invention, in logical formula (IV), two adjacent rings
GroupAdditional group can be passed through each other(in structural formula not
Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding)
And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon
Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R "
Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (IV), exist two with
On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups
GroupIn each with another adjacent cyclic groupFormed
The acridan ring.
According to the present invention, in logical formula (V), when having multiple, each group R is each other
It is identical or different, it is each independently selected from hydrogen, C1-300Straight or branched alkyl, logical formula (II)
Group shown in shown group and logical formula (III).
An embodiment of the invention, in logical formula (V), when having multiple,
Each group R is same to each other or different to each other, and is each independently selected from hydrogen and C1-300Straight or branched
Alkyl.
According to the present invention, in logical formula (V), as the C1-300Straight or branched alkane
Base, such as can enumerate C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkane
Base, more preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As the polyolefin
Base, specifically can such as enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000.
Now, as polyolefin-based number-average molecular weight Mn, preferred 500-2000 is more excellent
Select 500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is in
It is now chain alkyl structure), but depending on the polyolefinic species as initiation material or be somebody's turn to do
It is likely to containing a small amount of in the difference of polyolefin production process, the polyolefin-based strand
Olefinic double bond (such as in polyolefin manufacturing process remain or introduce), but this not shadow
The realization of sound effect of the present invention, the present invention also has no intention to carry out clearly the amount, and this
It is bright still polyolefin-based to classify as this " alkyl ".
, in logical formula (V), there are multiple groups in an embodiment of the invention
R, one of group R are described polyolefin-based, and another is hydrogen or C1-20Straight chain or
Branched alkyl (preferred C1-10Straight or branched alkyl, more preferably C1-4Straight or branched alkane
Base).
An embodiment of the invention, in logical formula (V), when group R is institute
When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (V).
According to the present invention, in logical formula (V), when having multiple, each group R' is each other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (V), when having multiple,
Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane
Base.
According to the present invention, in logical formula (V), group L is group
According to the present invention, in logical formula (V), in the definition of group L, group R "
Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up
Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (V), in determining for group L
In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous
Alkyl.
According to one preferred embodiment of the invention, in logical formula (V), in group L
Definition in, group R " selected from hydrogen and C1-10Straight or branched alkyl.
According to the present invention, in logical formula (V), two group R and group-(S)a-L-
Three positions of residue in logical formula (V) on phenyl ring are occupied respectively.
According to the present invention, in logical formula (V), a is 0 or 1, preferably 1.
According to the present invention, the shielding phenolic compounds is defined as previously mentioned (such as such as logical formula (I)
Or further as shown in logical formula (V)), it is necessary to comprising structureAs phenol unit.
According to one preferred embodiment of the invention, the shielding phenolic compounds is in its whole molecule
At most 5, at most 3, at most 2 or the at most 1 phenol list are included in structure
Unit.
According to the present invention, the shielding phenolic compounds is defined as previously mentioned (such as such as logical formula (II)
Or further as shown in logical formula (III) or (IV)), it is necessary to comprising structureAs amine unit.According to one preferred embodiment of the invention,
It is described shielding phenolic compounds in its whole molecular structure comprising at most 15, at most 10,
At most 8, at most 6, at most 4, at most 3 or the at most 2 amine lists
Unit.
According to the present invention, the shielding phenolic compounds in its whole molecular structure preferably at least
There is (preferably 2,3 or 4 or a more) group RdIt is hydrogen.It is concrete and
Speech, the shielding phenolic compounds is preferably in its whole molecular structure containing selected from following hydrogen amine
At least one of unit (1), hydrogen amine unit (2) and hydrogen amine unit (3).At these
In hydrogen amine unit, cyclic groupWith group R " with logical formula (II) in definition phase
Together.
A preferred embodiment of the invention, the shielding phenolic compounds is whole at its
Contain hydrogen amine unit (1) described at least one in molecular structure.
Specifically, shielding phenolic compoundsAs a example by, the compound
Comprising 2 phenol units and 2 amine units in its whole molecular structure, and wrap
Containing 1 hydrogen amine unit (1).
According to the present invention, as the shielding phenolic compounds, such as can enumerate following
The mixture of compound or its arbitrary proportion, but the present invention is not limited to this.
According to the present invention, the shielding phenolic compounds shown in aforementioned formula (I) can be with single
In the form of a kind of (pure) compound, manufacture or use, it is also possible to two of which or
In the form of various mixtures (in any proportion), manufacture or use, this not shadow
The realization of sound effect of the present invention.
According to the present invention, the shielding phenolic compounds shown in aforementioned formula (I) can by with
Under manufacture method manufactured, but be not limited to this sometimes.
The manufacture method of the invention, closes including the phenolate shown in logical formula (X) is made
Amines depositing in the aldehyde compound shown in formula (Z) shown in thing and formula (Y)
The first step reacted under.
According to the present invention, in leading to formula (X), when having multiple, each group R0It is mutually the same or
Difference, is each independently selected from hydrogen ,-SH and C1-300Straight or branched alkyl, on condition that
At least one group R0It is-SH.
According to the present invention, in logical formula (X), as the C1-300Straight or branched alkane
Base, such as can enumerate C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkane
Base, more preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As the polyolefin
Base, specifically can such as enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000.
Now, as polyolefin-based number-average molecular weight Mn, preferred 500-2000 is more excellent
Select 500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is in
It is now chain alkyl structure), but depending on the polyolefinic species as initiation material or be somebody's turn to do
It is likely to containing a small amount of in the difference of polyolefin production process, the polyolefin-based strand
Olefinic double bond (such as in polyolefin manufacturing process remain or introduce), but this not shadow
The realization of sound effect of the present invention, the present invention also has no intention to carry out clearly the amount, and this
It is bright still polyolefin-based to classify as this " alkyl ".
, in logical formula (X), there are multiple groups in an embodiment of the invention
R0, one of group R0It is-SH, two other group R0In one be described poly-
Alkylene, another is hydrogen or C1-20Straight or branched alkyl (preferred C1-10Straight chain is propped up
Alkyl group).
An embodiment of the invention, in logical formula (X), in group R0It is institute
When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (X).
According to the present invention, in logical formula (X), when having multiple, each group R' is each other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (X), when having multiple,
Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane
Base.
According to the present invention, as the phenolic compounds shown in the logical formula (X), can be direct
Using commercially available product, it is also possible to manufactured by conventionally known in the art method, and
Have no particular limits.In addition, as the phenolic compounds shown in the logical formula (X), can
With only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, as the manufacture method of the phenolic compounds shown in the logical formula (X),
Such as can enumerate in the presence of catalyst for alkylation reaction, make the phenol shown in formula (X')
(number-average molecular weight Mn is 300-3000, preferred 500-2000, more for compound and polyolefin
It is preferred that 500-1500) occur alkylated reaction method.
According to the present invention, in formula (X'), group R' has and aforementioned formula (X)
Middle identical implication.
According to three group R' of presence in the present invention, formula (X')0, one of group
R'0It is-SH, another group R'0It is H, the 3rd group R'0Be hydrogen ,-SH or
C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkyl).
An embodiment of the invention, in formula (X'), at least one group
R'0It is H, and group R'0The contraposition of phenolic hydroxyl group in formula (X').
According to the present invention, the polyolefin preferably passes through ethene, propylene or C4-C10Alpha-olefin
Homopolymerization or by polyolefin obtained from two or more copolymerization in these alkene.Make
For the C4-C10Alpha-olefin, such as can enumerate n-butene, isobutene, n-pentene, just
Hexene, positive octene and positive decene.
According to the present invention, at least 20wt% in these polyolefin (preferably at least 50wt%,
More preferably at least 70wt%) polymer chain contain olefinic double bond in its end.The olefinic is double
Key is usually in the form of the ethenylidene or vinyl of high reaction activity.
According to the present invention, as the polyolefin, more preferably polybutene.Unless otherwise stated,
Term as used herein " polybutene " is broadly included by 1- butylene or isobutylene homopolymerisation
The polymer for obtaining, and led to by two or three in 1- butylene, 2- butylene and isobutene
Cross copolymerization and obtained polymer.The commercially available prod of such polymer is likely to containing negligible
Other olefinic components of amount, but this has no effect on the enforcement of the present invention.
According to the present invention, as the polyolefin, further preferred polyisobutene (PIB),
Also referred to as high-activity polyisobutylene.In this kind of polyisobutene, at least 20wt% is (excellent
Choosing at least 50wt%, more preferably at least 70wt%) total terminal ethylenic double bond be by methyl
What ethenylidene was provided.
As the catalyst for alkylation reaction, such as Lewis acid catalysts can be enumerated,
Such as it is selected from alchlor, boron trifluoride, butter of tin, titanium tetrabromide, boron trifluoride benzene
One or more in phenol, boron trifluoride alcohol complex and boron trifluoride ether complex, its
In preferably boron trifluoride etherate and/or boron trifluoride methanol complex compound.These alkyl
Changing catalysts can directly use commercially available product.
According to the present invention, in the alkylated reaction, the polyolefin, the formula (X')
Mol ratio between shown phenolic compounds, the catalyst for alkylation reaction such as can be
1:1-3:0.1-0.5, preferably 1:1.5-3:0.1-0.4, most preferably 1:1.5-3:0.2-0.4,
But this is not limited to sometimes.
According to the present invention, the reaction time of the alkylated reaction is such as 0.5h-10h, excellent
1h-8h, most preferably 3h-5h are selected, but is not limited to this sometimes.
According to the present invention, the reaction temperature of the alkylated reaction is such as 0 DEG C -200 DEG C,
It is preferred that 10 DEG C -150 DEG C, most preferably 20 DEG C -100 DEG C, but this is not limited to sometimes.
According to the present invention, the alkylated reaction can be carried out in the presence of the solvent.As
The solvent, such as can enumerate C6-10Alkane (such as hexane, heptane, octane, nonyl
Alkane or decane etc.).Wherein, hexane and heptane are preferably used, more preferably using hexane.
According to the present invention, after the alkylated reaction terminates, by conventional methods from final
Catalyst for alkylation reaction, unreacted reactant and can are removed in the reactant mixture of acquisition
After the solvent that can be used, that is, obtain the phenolic compounds shown in the logical formula (X).
According to the present invention, in formula (Y), group R'2Selected from hydrogen, C1-20Straight chain or
Branched alkyl and group
According to the present invention, in formula (Y), when having multiple, each group RbEach other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl, it is preferably each
From independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in formula (Y), when having multiple,
Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched
Alkyl, preferred hydrogen.
According to the present invention, in formula (Y), when having multiple, each group RcEach other
It is identical or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly
Chain or branched alkyl epoxide.
An embodiment of the invention, in formula (Y), when having multiple,
Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched
Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in formula (Y), preferably one group
RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding)
Contraposition.
According to the present invention, in formula (Y), y is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in formula (Y), z is 0 to 3 integer, preferably 0 or
1。
According to the present invention, in formula (Y), n1 is 1 to 8 integer, preferably 1 or
2。
According to the present invention, in formula (Y), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of formula (Y)) is mutually the same
Or it is different, (inside configuration preferably in formula (Y) is presented to be each independently selected from phenyl ring
For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in formula (Y) is rendered as 1,4-
Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
According to the present invention, as the amines shown in the formula (Y), can be direct
Using commercially available product, it is not particularly limited.In addition, as the formula (Y)
Shown amines, can only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in formula (Z), group R " it is selected from hydrogen, C1-20Alkyl is (excellent
Select C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in formula (Z), group R " selected from hydrogen,
C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl.
According to one preferred embodiment of the invention, in formula (Z), group R "
Selected from hydrogen and C1-10Straight or branched alkyl.
According to the present invention, as the aldehyde compound shown in the formula (Z), such as can be with
Enumerate C1-6Aliphatic aldehyde and benzaldehyde.
An embodiment of the invention, as the C1-6Aliphatic aldehyde, such as may be used
To enumerate C1-6Straight or branched saturated aliphatic aldehyde, specifically such as acetaldehyde or formaldehyde, more preferably
Formaldehyde.As the formaldehyde, such as can use its aqueous solution, paraformaldehyde or oligomeric first
Aldehyde form, is not particularly limited.
According to the present invention, as the aldehyde compound shown in the formula (Z), can only make
With one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first
In step, the phenolic compounds shown in the logical formula (X) with shown in the formula (Y)
The mol ratio of amines is generally 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first
In step, the phenolic compounds shown in the logical formula (X) with shown in the formula (Z)
The mol ratio of aldehyde compound is generally 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the first step
Suddenly can carry out in the presence of the solvent.As the solvent, such as can enumerate C2-10
Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon (such as benzene,toluene,xylene and
Isopropylbenzene), C6-10Alkane (such as n-hexane, hexamethylene and petroleum ether), C1-6Aliphatic
Alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropanol, n-butanol and ethylene glycol), C2-20
Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride, chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone
(such as acetone, butanone and methyl iso-butyl ketone (MIBK)) or C3-10Acid amides (such as dimethyl
Formamide, dimethyl acetamide and 1-METHYLPYRROLIDONE) etc..These solvents can be only
Using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first
In step, catalyst can be added without, it is also possible to add catalyst.As the catalyst,
Inorganic acid catalyst and organic acid catalyst can such as be enumerated.As the inorganic acid catalysis
Agent, such as can enumerate hydrochloric acid, sulfuric acid and phosphoric acid etc..As the organic acid catalyst,
Pyrovinic acid, ethylsulfonic acid, sulfamic acid and p-methyl benzenesulfonic acid etc. can such as be enumerated.
As the consumption of the catalyst, can directly with reference to the conventional amount used of prior art,
It is not particularly limited.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described first
The reaction time of step, there is no particular limitation, but generally 0.1h-24h, preferred 0.2h-12h,
Most preferably 0.5h-6h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described first
There is no particular limitation for the reaction temperature of step, but generally 0 DEG C -250 DEG C, preferably
20 DEG C -180 DEG C, most preferably 60 DEG C -120 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first
After step terminates, by conventionally known separation method (such as evaporation etc.) from this first
Remove in the reactant mixture (the hereinafter referred to as reactant mixture of first step) that step is obtained
After the volatile materials such as solvent that may be present, you can obtain the product of first step.
An embodiment of the invention, the manufacture method of the shielding phenolic compounds is appointed
Choosing also includes making the product of the first step and vulcanizing agent reaction (forming phenthazine ring)
Additional step (hereinafter referred to as additional step A).
An embodiment of the invention, the manufacture method of the shielding phenolic compounds is appointed
Choosing also includes making the product of the first step and the hydroformylation shown in aforementioned formula (Z)
Additional step (the hereinafter referred to as extra step of compound reaction (formed acridan ring)
Rapid B).
According to the present invention, in the manufacture method of the shielding phenolic compounds, can only carry out
The additional step A, it is also possible to only carry out the additional step B, it is also possible to both carried out institute
State additional step A carries out the additional step B again.Both the additional step A is being carried out
When carrying out the additional step B again, to the additional step A and additional step B
Precedence there is no particular limitation, can first carry out the additional step A, it is attached at this
Plus step A terminates to carry out the additional step B again afterwards, or first carry out the extra step
Rapid B, after additional step B terminates the additional step A is carried out again.In addition, each
There can be product (that is, from the product of previous additional step) point between additional step
From step, it is also possible to there is no product separating step, be not particularly limited.
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds
In, the additional step A is carried out after the first step terminates.Now, it is described
The product of first step is as previously mentioned from the reactant mixture of the first step
In separate.Or, the product of the first step can also without the separation,
And be directly used to carry out the extra step in the form of the reactant mixture of the first step
Rapid A.Or, the additional step A can also be after the additional step B terminates
Carry out.When the additional step A after the additional step B terminates when carrying out, institute
The product for stating additional step B is as described herein from the anti-of the additional step B
Answer in mixture and separate.Or, the product of the additional step B can also
Without the separation, and directly used in the form of the reactant mixture of the additional step B
In carrying out the additional step A.
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds
In, in the additional step A, as the vulcanizing agent, such as can enumerate sulphur and
Sulfur dichloride etc., wherein it is preferred that sulphur.As the sulphur, such as can enumerate sulphur or distillation
Sulphur.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
In step A, the mol ratio of the amines shown in the formula (Y) and the vulcanizing agent
Generally 1:1-10, preferably 1:1.2-6.0, more preferably 1:1.5-3.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step
Rapid A can be carried out in the presence of the solvent.As the solvent, such as can enumerate C2-10
Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon (such as benzene,toluene,xylene and
Isopropylbenzene), C6-10Alkane (such as n-hexane, hexamethylene and petroleum ether), C1-6Aliphatic
Alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropanol, n-butanol and ethylene glycol), C2-20
Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride, chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone
(such as acetone, butanone and methyl iso-butyl ketone (MIBK)) or C3-10Acid amides (such as dimethyl
Formamide, dimethyl acetamide and 1-METHYLPYRROLIDONE) etc..These solvents can be only
Using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step
Rapid A is typically carried out in the presence of a catalyst.As the catalyst, such as can lift
The have technology conventional catalyst for adopting for this purpose, specifically such as iodine.As described
The consumption of catalyst, can directly with reference to prior art conventional amount used, not particularly
Limit.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional
The reaction time of step A, there is no particular limitation, but generally 0.1h-24h, preferably
0.2h-12h, most preferably 0.5h-4h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional
There is no particular limitation for the reaction temperature of step A, but generally 60 DEG C -300 DEG C, preferably
120 DEG C -240 DEG C, most preferably 150 DEG C -200 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
After step A terminates, by conventionally known separation method (such as evaporation etc.) from this
The volatility thing such as solvent that may be present is removed in the reactant mixture that additional step A is obtained
After matter, you can obtain the product of additional step A, or can also be without this
Separate, be directly used in follow-up reactions steps (than additional step B as the aforementioned).
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds
In, the additional step B can be carried out (as list after the first step terminates
Only step), it is also possible to carry out simultaneously with the first step, be not particularly limited.
When the additional step B after the first step terminates when carrying out, the first step
The separation from the reactant mixture of the first step as previously mentioned of rapid product
Out.Or, the product of the first step can also be and straight without the separation
To connect be used in the form of the reactant mixture of the first step and carry out the additional step B.
Or, the additional step B can also be carried out after the additional step A terminates.
It is described additional when the additional step B after the additional step A terminates when carrying out
The reaction from the additional step A as described herein of the product of step A mixes
Separate in thing.Or, the product of the additional step A can also be without
The separation, and be directly used to carry out in the form of the reactant mixture of the additional step A
The additional step B.In addition, when simultaneously the additional step B enters with the first step
During row, directly in the reaction system of the first step (such as in the first step
Start or during the first step is carried out) add institute according to hereinafter provided consumption
State the aldehyde compound shown in formula (Z).
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
In step B, as the aldehyde compound shown in the formula (Z), such as can enumerate
C1-6Aliphatic aldehyde and benzaldehyde.As the C1-6Aliphatic aldehyde, such as can enumerate C1-6
Straight or branched saturated aliphatic aldehyde, specifically such as acetaldehyde or formaldehyde, more preferably formaldehyde.As
The formaldehyde, such as can use its aqueous solution, paraformaldehyde or paraformaldehyde form, and
There is no particular limitation.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
In step B, the amines shown in the formula (Y) with the formula (Z) Suo Shi
The mol ratio of aldehyde compound be generally 1:0.1-10, preferably 1:0.5-5.0, more preferably
1:0.8-2.0。
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step
Rapid B (when carrying out as independent step) can be carried out in the presence of the solvent.As institute
Solvent is stated, such as can enumerate C2-10Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon
(such as benzene,toluene,xylene and isopropylbenzene), C6-10Alkane (such as n-hexane, ring
Hexane and petroleum ether), C1-6Aliphatic alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropyl
Alcohol, n-butanol and ethylene glycol), C2-20Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride,
Chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone (such as acetone, butanone and methyl iso-butyl ketone (MIBK))
Or C3-10Acid amides (such as dimethylformamide, dimethyl acetamide and N- methylpyrroles
Alkanone) etc..These solvents can only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
In step B (when carrying out as independent step), catalyst can be added without, it is also possible to
Add catalyst.As the catalyst, such as can enumerate inorganic acid catalyst and organic
Acid catalyst.As the inorganic acid catalyst, such as can enumerate hydrochloric acid, sulfuric acid and phosphorus
Acid etc..As the organic acid catalyst, such as can enumerate pyrovinic acid, ethylsulfonic acid,
Sulfamic acid and p-methyl benzenesulfonic acid etc..As the consumption of the catalyst, can directly reference
The conventional amount used of prior art, is not particularly limited.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional
The reaction time of step B (when carrying out as independent step), there is no particular limitation, but
Generally 0.1h-24h, most preferably preferred 0.2h-12h, 0.5h-6h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional
There is no particular limitation for the reaction temperature of step B (when carrying out as independent step), but
Generally 0 DEG C -250 DEG C, preferably 20 DEG C -180 DEG C, most preferably 60 DEG C -120 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional
After step B (when carrying out as independent step) terminates, by conventionally known separation
Removing in the reactant mixture that method (such as evaporation etc.) is obtained from additional step B can
After the volatile materials such as the solvent that can exist, you can the reaction for obtaining additional step B is produced
Thing, or follow-up reactions steps can also be directly used in (before such as without the separation
The additional step A for stating).
It is known in the art, aforementioned all of reactions steps (including the first step,
The additional step A and additional step B) it is general under the protection of inert gas atmosphere
Carry out.As the inert gas, such as nitrogen and argon gas etc. can be enumerated, it is not special
Other restriction.
According to the present invention, in the manufacture method of the shielding phenolic compounds, as described the
The product of one step, the product of the additional step A or the additional step
The product of B, can be a kind of single shielding phenolic compounds (such as aforementioned formula (I)
Shown shielding phenolic compounds), or the mixture comprising various shielding phenolic compounds.
These product are all that desired by the present invention, the difference of its existence form has no effect on this
The realization of invention effect.Therefore, in this specification context these are reacted without distinction
Product is collectively termed as the shielding phenolic compounds of the present invention.In consideration of it, according to the present invention, not
Presence is further purified these product, or further separates from these product
The absolute necessity for going out the shielding phenolic compounds of a certain ad hoc structure.Certainly, the purifying or point
It is preferred from being sometimes for the further lifting of Expected Results of the present invention, but Yu Benfa
For bright not necessarily.Even so, as the purifying or separation method, such as can be with
Enumerate the product is purified by methods such as column chromatography method or preparative chromatographies
Or separate etc..
An embodiment of the invention, further relates to according to aforesaid shielding phenol of the invention
The shielding phenolic compounds of the manufacture method manufacture of compound.
The present invention's shields phenolic compounds due to showing excellent high-temperature oxidation resistance, because
This is particularly suitable as antioxidant and uses, and is used for manufacture especially as antioxidant and expects excellent
(high temperature) oxidation stability lubricant oil composite.In consideration of it, of the invention one
Individual embodiment, is related to a kind of industrial lubrication fluid composition, and it includes aforesaid of the present invention
What shielding phenolic compounds (or mixture of its arbitrary proportion), extreme pressure anti-wear additives, metal subtract
Agent living, antirust agent and lube base oil.
Embodiment
Hereinafter the present invention is illustrated in further detail using embodiment, but the present invention is not limited to
These embodiments.
Performance in embodiment and comparative example is evaluated as follows.
(1) high-temperature oxidation resistance evaluation
The lubricant oil composite that embodiment or comparative example are manufactured is adopted and added as test specimen
Pressure differential scanning calorimetry (PDSC) evaluates the antioxygenic property of the test specimen, to try
The oxidation induction period (unit is min) for testing sample is represented.The temperature of PDSC tests is 210 DEG C,
Pressure is 0.5MPa, and oxygen gas flow rate is 100mL/min.
(2) deposit generates rejection evaluation
The lubricant oil composite that embodiment or comparative example are manufactured is carried out into mould as test specimen
Intend the engine crankcase coking simulated test of piston deposit.The method is by 300ml
Test specimen adds coking plate analog meter, 150 DEG C is heated to, using continuation mode to temperature
For 310 DEG C of aluminium sheet spilled oil, the burnt amount generated on aluminium sheet is weighed after 6 hours, to deposit
Thing amount (unit is mg) expression, simulates the deposit on piston.Coking amount is higher, generation
The piston detergency of table this test specimen is poorer.
(3) extreme pressure property evaluation
According to GB/T12583-1998 standard methods, the profit that embodiment or comparative example are manufactured
Sliding oil composition carries out extreme pressure property evaluation as test specimen.Experimental condition is the speed of mainshaft
1760r/min, 18~35 DEG C of sample temperature.Increase load step by step from 784N open types, do one
The 10s tests of series, the measured wear scar diameter of record, until sintering.To test survey
Sintering load evaluating the extreme pressure property of sample.
(4) wear resistance evaluation
According to SH/T0189-1992 standard methods, the lubrication that embodiment or comparative example are manufactured
Fluid composition carries out wear resistance evaluation as test specimen.The test bar of wear-resistant test
Part is the effect of 392N (40kg) power, 75 DEG C of oil sump temperature, and head a ball rotating speed 1200r/min,
Time 60min.The wear resistance of sample passes through the average of the wear scar diameter of following three balls
Value is evaluating.
(5) high-frequency reciprocating friction test antifriction performance evaluation
The lubricant oil composite that embodiment or comparative example are manufactured is carried out into height as test specimen
Frequency reciprocating friction is tested.The experimental condition of the method is to load 1000g, frequency 20Hz,
100 DEG C of temperature, test period is 60min, records coefficient of friction.Coefficient of friction is less,
Show that the antifriction performance of test specimen is better.
(6) copper corrosion assessment of performance is suppressed
With reference to ASTM D130 standard methods, the lubricating oil that embodiment or comparative example are manufactured
Composition carries out copper strip test as test specimen.The copper sheet for having polished is immersed in into examination
In sample, 121 DEG C of test temperature is heated to, is kept for 3 hours, end to be tested, take out copper
Piece, it is scrubbed to be compared with Corrosion standards colour table afterwards, determine corrosion level.
(7) rustless property evaluation
According to the standard methods of GB/T 11143, the lubricating oil that embodiment or comparative example are manufactured
Composition carries out antiseptic property test as test specimen.By 300mL samples and 30mL
Distilled water mixes, and test rod iron is totally immersed into wherein, stirs 24 hours at 60 DEG C,
The vestige of viewing test rod iron corrosion and the degree of corrosion after off-test.
Embodiment 1
In the 500ml four-hole boiling flasks equipped with agitator, thermometer, condenser pipe and dropping funel
In, add 58.79g (0.323mol) the 2- tert-butyl group -6- mercapto-phenols, 6.88g (0.048mol)
BFEE (catalyst for alkylation reaction), 100ml n-hexanes solvent and
(Mn=1000, Jilin Chemical group fine chemicals has the polyisobutene of 161.61g (0.162mol)
Limit company manufactures), react 2h at 80 DEG C.After reaction terminates, use quality fraction is 5%
Potassium hydroxide solution cleaning reactant mixture once, and with hot water be washed to neutrality to remove
Catalyst, then vacuum distillation removes solvent and unreacted phenol, obtains polyisobutene sulfydryl
Phenol, hydroxyl value is 53.49mgKOH/g.Hydroxy value measuring is with reference in GB/T7383-2007
Acetic anhydride method.
Example reaction equation is as follows:
From the nucleus magnetic hydrogen spectrum spectrum analysis of polyisobutene mercapto-phenol product:Chemical shift
It is the characteristic peak of tert-butyl group hydrogen on polyisobutene mercapto-phenol phenyl ring at 1.40;Chemical shift
The unimodal characteristic peak for sulfydryl hydrogen on polyisobutene mercapto-phenol phenyl ring at 3.58;Chemical shift
The unimodal characteristic peak for hydroxyl hydrogen on polyisobutene mercapto-phenol phenyl ring at 4.84;Chemical shift
At 7.12 it is unimodal and 7.20 at it is unimodal be respectively polyisobutene mercapto-phenol phenyl ring on two hydrogen
Characteristic peak.It is 1 by the Definitions On Integration of hydroxyl hydrogen on phenyl ring, obtains hydrogen on phenyl ring, sulfydryl
The integration of hydrogen and hydroxyl hydrogen compares for 0.95:0.97:1.05:0.94, it is close to theoretical 1:1:1:1:1,
From nuclear magnetic spectrogram analysis, the polyisobutene mercapto-phenol alkyl that expected contraposition replaces is synthesized
Change product.
Embodiment 2
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 30.58 grams of (156mmol) 2- sulfydryl -4- methyl -6-
Methylphenol, 9.29 grams of (112mmol) formaldehyde, 32.38 grams of (176mmol) N- benzene
Base p-phenylenediamine and 100mL toluene, rapid stirring, at 100 DEG C 2h is reacted.Question response
After end, vacuum distillation removes solvent and a small amount of water for generating, and is obtained by column chromatography for separation
To the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.40 (9H), 2.37 (3H), 4.02
(1H), 4.83 (2H), 6.95-7.00 (12H), 7.26 (2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 21.2,30.1,34.1,49.9,114.3,
118.9,119.4,121.8,122.2,125.8,126.5,129.5,131.8,132.3,
133.5,143.3,150.8;
C24H28N2OS calculated values C 73.43, H 7.19, N 7.14, O 4.08, S 8.17;
Measured value:C 73.31, H 7.23, N 7.21, O 3.99, S 8.28.
Embodiment 3
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 31.65 grams of (133mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 1.86 grams of (62mmol) formaldehyde, 28.15 grams of (153mmol) N- phenyl
P-phenylenediamine, 0.75 gram of (7.5mmol) hydrochloric acid and 150mL isopropanols, rapid stirring,
24h is reacted at 25 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent
Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36-1.54 (18H), 3.75 (1H),
4.80 (2H), 5.32 (1H), 6.80 (2H), 6.97 (5H), 7.17 (2H), 7.26
(2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,51.2,119.4,121.8,
126.5,129.5,131.4,136.6,144.5,153.4;
C27H34N2OS calculated values C 74.61, H 7.88, N 6.45, O 3.68, S 7.38;
Measured value:C 74.52, H 7.84, N 6.51, O 3.73, S 7.40.
Embodiment 4
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 8.57 grams of (36mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 1.24 grams of (15mmol) formaldehyde, 10.14 grams of (39mmol) N, N'- bis-
Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring, at 90 DEG C 4h is reacted.Treat anti-
After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation
Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 5.23 (2H), 6.80-7.02
(10H), 7.17 (2H), 7.26 (4H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,55.2,117.1,121.8,
126.2,129.5,136.6,143.6,153.4;
C33H38N2OS calculated values C 77.60, H 7.50, N 5.48, O 3.13, S 6.28;
Measured value:C 77.71, H 7.52, N 5.53, O 3.10, S 6.23.
Embodiment 5
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 20.23 grams of (85mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 9.54 grams of (115mmol) formaldehyde, 18.49 grams of (69mmol) N- (1,3-
Dimethylbutyl)-N'- diphenyl-para-phenylene diamines and 150mL benzene, rapid stirring is anti-at 85 DEG C
Answer 3h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and leads to
Cross the shielding phenol product that column chromatography for separation obtains structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 0.80 (6H), 1.11-1.21 (4H),
1.36 (18H), 1.67 (2H), 3.47 (1H), 4.80 (2H), 5.32 (1H), 6.80
(2H), 6.97 (5H), 7.17 (2H), 7.26 (2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 17.9,22.4,29.6,34.6,45.2,
52.7,58.6,119.4,121.8,126.2,129.5,131.2,136.6,144.1,
146.1,153.4;
C33H46N2OS calculated values:C 76.40, H 8.94, N 5.40, O 3.08, S 6.18;
Measured value:C 76.48, H 8.96, N 5.35, O 3.09, S 6.12.
Embodiment 6
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 3.57 grams of (15mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 5.14 grams of (62mmol) formaldehyde, 21.76 grams of (103mmol) N- phenyl
- N '-[4- (phenyl amino) phenyl]-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring,
2h is reacted at 110 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent
Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 5.20 (2H), 5.32
(1H), 6.80-7.02 (14H), 7.17 (2H), 7.20 (1H), 7.26 (4H),
7.55(1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,55.5,117.1,120.4,
126.2,129.5,132.3,136.6,142.8,146.1,153.4;
C36H43N3OS calculated values C 77.83, H 7.20, N 6.98, O 2.66, S 5.33;
Measured value:C 77.69, H 7.19, N 7.08, O 2.65, S 5.38.
Embodiment 7
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 34.51 grams of (145mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 2.91 grams of (35mmol) formaldehyde, 4.49 grams of (21mmol) 4- amino -4'-
Methoxy diphenylamine, 0.26 gram of (2.61mmol) hydrochloric acid and 150mL benzene, rapid stirring,
2h is reacted at 90 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent
Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 3.72-3.76 (4H),
4.80 (2H), 5.32 (1H), 6.97-7.06 (8H), 7.17 (2H), 7.20 (1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,51.1,55.5,114.6,
118.9,121.8,124.7,126.5,132.3,136.6,144.5,153.4,154.5;
C28H36N2O2S calculated values C 72.38, H 7.81, N 6.03, O 6.89, S 6.90;
Measured value:C 72.37, H 7.69, N 6.12, O 6.80, S 6.83.
Embodiment 8
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add gram 21.66 (91mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 1.35 grams of (9.51mmol) aldehyde C-9s, 6.51 grams of (25mmol) N, N'- bis-
Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL benzene, rapid stirring, at 70 DEG C 6h is reacted.Question response
After end, vacuum distillation removes solvent and a small amount of water for generating, and is obtained by column chromatography for separation
To the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 0.88 (3H), 1.08-1.85 (24H),
5.23 (1H), 5.32 (1H), 6.80 (1H), 6.97 (8H), 7.17 (2H), 7.26
(4H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 14.1,22.6,29.6,31.7,34.6,
41.6,60.8,116.6,119.4,121.8,126.5,129.5,131.4,136.6,
142.8,144.5,146.1,153.4;
C38H48N2OS calculated values C 78.57, H 8.33, N 4.82, O 2.75, S 5.52;
Measured value:C 78.62, H 8.25, N 4.75, O 2.81, S 5.42.
Embodiment 9
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 8.33 grams of (35mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 4.23 grams of (51mmol) formaldehyde, 9.61 grams of (31mmol) N, N'- hexichol
Base -2,6- naphthylenediamines and 150mL toluene, rapid stirring, at 110 DEG C 4h is reacted.Treat anti-
After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation
Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 5.25 (2H), 5.32
(1H), 5.80 (1H), 6.99-7.06 (7H), 7.17 (3H), 7.26 (4H), 7.40
(2H), 7.84 (2H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,54.8,106.9,118.6,
123.3,126.2,129.2,136.6,142.8,148.3,153.5;
C37H41N2OS calculated values C 79.24, H 7.19, N 5.00, O 2.85, S 5.72;
Measured value:C 79.20, H 7.23, N 5.14, O 2.72, S 5.65.
Embodiment 10
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 6.19 grams of (26mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 9.57 grams of (92mmol) 3- methylthiopropionaldehyde aldehyde, 3.13 grams (17mmol)
4-aminodiphenylamine and 150mL toluene, rapid stirring, at 80 DEG C 2h is reacted.Treat
After reaction terminates, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography point
From the shielding phenol product for obtaining structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36-1.54 (18H), 2.12-2.80 (7H),
3.47 (1H), 4.97 (1H), 5.32 (1H), 6.97 (7H), 7.17 (2H), 7.26
(2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 15.2,29.6,31.9,34.6,41.7,
60.2,114.3,119.4,121.8,126.2,129.5,132.4,136.6,144.5,
146.1,153.5;
C30H40N2OS2Calculated value C 70.82, H 7.92, N 5.51, O 3.14, S 12.60;
Measured value:C 70.75, H 7.83, N 5.46, O 3.20, S 12.71.
Embodiment 11
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 4.99 grams of (21mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 4.4 grams of (53mmol) formaldehyde, 5.70 grams of (31mmol) N- phenyl pair
Phenylenediamine and 150mL ethanol, rapid stirring after reacting 2.5h at 60 DEG C, is down to room temperature,
7.05 grams of (85mmol) formaldehyde are added, 85 DEG C of reaction 2.5h are warming up to.Question response terminates
Afterwards, vacuum distillation removes solvent and a small amount of water for generating, and is marked by column chromatography for separation
The shielding phenol product of structure shown in topic.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 3.74 (1H), 4.12
(2H), 4.59 (1H), 4.83 (2H), 5.32 (1H), 6.97-7.11 (5H), 7.17
(2H), 7.24 (2H);
13C NMR (75MHz, CDCl3):δ 29.6,33.1,34.6,50.6,119.4,
123.3,126.2,126.7,127.9,136.6,140.5,142.9,153.4;
C26H34N2OS calculated values C 75.29, H 7.67, N 6.27, O 3.58, S 7.18;
Measured value:C 75.20, H 7.59, N 6.29, O 3.65, S 7.22.
Embodiment 12
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 19.52 grams of (82mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 10.04 grams of (121mmol) formaldehyde, 19.93 grams of (94mmol) 4- amino
- 4'- ethyls diphenylamines and 150mL dimethylbenzene, rapid stirring, after reacting 3h at 90 DEG C,
Room temperature is down to, 10.11 grams of (316mmol) sulphur and 0.04 gram of (0.35mmol) iodine is added,
It is warming up to 150 DEG C of reaction 8h.After question response terminates, vacuum distillation removes solvent with generation
A small amount of water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.23 (1H), 1.36 (18H), 2.61
(2H), 3.77 (1H), 4.84 (2H), 5.32 (1H), 5.70 (1H), 6.98 (5H),
7.17 (2H), 7.49 (1H);
13C NMR (75MHz, CDCl3):δ 15.60,29.6,34.6,50.7,118.9,
121.8,126.2,129.7,136.6,141.2,146.1,153.4;
C29H36N2OS2Calculated value C 70.69, H 7.36, N 5.69, O 3.25, S 13.02;
Measured value:C 70.77, H 7.41, N 5.67, O 3.17, S 12.93.
Embodiment 13
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 10.95 grams of (46mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 3.98 grams of (48mmol) formaldehyde, 13.78 grams of (53mmol) N, N'- bis-
Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL trimethylbenzenes, rapid stirring, after reacting 1h at 85 DEG C,
3.82 grams of (46mmol) formaldehyde are added, after continuing to react 1h at 85 DEG C, room temperature is down to,
10.11 grams of (316mmol) sulphur and 0.27 gram of (2.11mmol) iodine are added, 180 DEG C are warming up to
Reaction 1h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and
The shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 4.26 (2H), 5.18
(2H), 5.32 (1H), 6.40 (1H), 6.97 (8H), 7.17 (2H), 7.37 (2H);
13C NMR (75MHz, CDCl3):δ 29.6,33.6,34.6,54.3,106.5,
114.4,119.4,121.8,126.2,129.5,136.6,141.9,144.5,153.4;
C34H36N2OS2Calculated value C 73.87, H 6.56, N 5.07, O 2.89, S 11.60;
Measured value:C 73.91, H 6.49, N 5.02, O 2.94, S 11.49.
Embodiment 14
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 21.66 grams of (91mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 7.39 grams of (89mmol) formaldehyde, 6.62 grams of (36mmol) N- phenyl pair
Phenylenediamine, 0.45 gram of (4.51mmol) NaOH and 150mL isopropanols, stir rapidly
Mix, at 80 DEG C 3h is reacted.After question response terminates, vacuum distillation removes solvent with generation
A small amount of water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36-1.54 (36H), 4.82 (4H),
5.32 (2H), 6.97 (7H), 7.17 (4H), 7.26 (2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,56.5,106.5,119.4,
121.8,126.5,129.5,131.4,136.6,144.5,146.1,153.4;
C42H56N2O2S2Calculated value C 73.64, H 8.24, N 4.09, O 4.67, S 9.36;
Measured value:C 73.59, H 8.21, N 4.15, O 4.62, S 9.34.
Embodiment 15
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 6.55 grams of (36mmol) 2- tert-butyl group -4- sulfydryl benzene
Phenol, 7.64 grams of (92mmol) formaldehyde, 13.06 grams of (71mmol) N- phenyl are to benzene two
Amine and 150mL toluene, rapid stirring, at 90 DEG C 4h is reacted.After question response terminates, subtract
Pressure is distilled off solvent and a small amount of water for generating, and is obtained shown in title by column chromatography for separation
The shielding phenol product of structure.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (9H), 3.81 (1H), 4.38
(2H), 4.69 (2H), 5.29 (1H), 6.95-7.00 (15H), 7.17 (1H),
7.26 (4H), 7.55 (1H), 8.62 (1H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,43.5,50.8,114.3,
119.4,121.8,125.4,129.5,132.3,136.6,145.2,146.1,149.0,
153.4;
C36H38N4OS calculated values C 75.23, H 6.66, N 9.75, O 2.78, S 5.58;
Measured value:C 75.27, H 6.69, N 9.68, O 2.79, S 5.51.
Embodiment 16
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 11.66 grams of (49mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 10.92 grams of (53mmol) 2,6- DI-tert-butylphenol compounds, 7.89 grams (95mmol)
Formaldehyde, 11.23 grams of (32mmol) N- phenyl-N '-[4- (phenyl amino) phenyl]-Isosorbide-5-Nitraes-
Phenylenediamine and 150mL toluene, rapid stirring, at 100 DEG C 3h is reacted.Question response terminates
Afterwards, vacuum distillation removes solvent and a small amount of water for generating, and is marked by column chromatography for separation
The shielding phenol product of structure shown in topic.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36-1.54 (36H), 4.91 (2H),
5.22 (2H), 5.32 (2H), 6.97-7.07 (16H), 7.17 (2H), 7.20 (1H),
7.27(4H);
13C NMR (75MHz, CDCl3):δ 29.6,34.4,55.6,56.9,93.6,
119.4,123.3,126.5,129.2,131.4,136.6,142.8,146.1,153.4;
C54H65N3O2S calculated values C 79.08, H 7.99, N 5.12, O 3.90, S 3.91;
Measured value:C 79.15, H 8.03, N 5.01, O 3.87, S 3.85.
Embodiment 17
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 47.16 grams of (45mmol) polyisobutene mercapto-phenols
(embodiment 1 is manufactured), 4.23 grams of (51mmol) formaldehyde, 9.75 grams (53mmol)
4-aminodiphenylamine and 150mL benzene, rapid stirring, at 80 DEG C 2.5h is reacted.Treat anti-
After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation
Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 0.88,0.98,1.02,1.24,1.40,
2.42,4.86,6.97,7.02,7.14,7.26,7.55;
13C NMR (75MHz, CDCl3):δ 28.2,30.1,32.3,34.5,38.1,
49.8,59.1,114.3,119.4,121.8,122.0,127.3,129.5,132.3,
143.3,146.1,151.3.
Embodiment 18
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 29.34 grams of (28mmol) polyisobutene mercapto-phenols
(embodiment 1 is manufactured), 2.91 grams of (35mmol) formaldehyde, 6.24 grams (24mmol)
N, N'- diphenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring, in 90 DEG C of reactions
2h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and by post
Chromatography obtains the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 0.88,0.98,1.02,1.24,1.40,
2.42,4.00,4.86,5.56,6.97,7.02,7.14,7.26,7.55;
13C NMR (75MHz, CDCl3):δ 28.2,30.1,32.3,33.1,34.5,
38.1,49.8,59.1,114.3,119.4,121.8,125.2,122.0,127.3,129.5,
132.3,143.3,146.1,151.3.
Comparative example 1
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 20.23 grams of (85mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 7.22 grams of (87mmol) formaldehyde, 14.37 grams of (85mmol) diphenylamines
With 150mL methyl alcohol, rapid stirring, at 60 DEG C 2h is reacted.After question response terminates, decompression
Solvent and a small amount of water for generating are distilled off, and obtain being tied shown in title by column chromatography for separation
The shielding phenol product of structure.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.36 (18H), 5.21 (2H), 5.32
(1H), 6.99 (6H), 7.17 (2H), 7.27 (4H);
13C NMR (75MHz, CDCl3):δ 29.6,34.6,55.2,120.4,123.3,
125.9,126.2,129.2,136.6,150.0,153.5;
C27H33NOS calculated values C 77.28, H 7.93, N 3.34, O 3.81, S 7.64;
Measured value:C 77.22, H 7.89, N 3.31, O 3.83, S 7.67.
Comparative example 2
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 10.71 grams of (52mmol) 2,6- di-t-butyl -4-
Mercapto-phenol, 1.89 grams of (63mmol) formaldehyde, 17.42 grams of (65mmol) N- (1,3-
Dimethylbutyl)-N'- diphenyl-para-phenylene diamines and 150mL methyl alcohol, rapid stirring, at 70 DEG C
Reaction 4h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and
The shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 0.80 (6H), 1.11 (3H), 1.29
(1H), 1.36 (18H), 3.45 (1H), 4.53 (2H), 5.32 (2H), 6.97-7.07
(9H), 7.26 (2H), 7.55 (1H);
13C NMR (75MHz, CDCl3):δ 17.9,22.40,24.6,30.4,34.3,
45.7,54.5,56.7,116.6,120.4,121.8,125.9,128.9,129.5,135.6,
146.1,153.5,154.8;
C33H46N2O calculated values C 81.43, H 9.53, N 5.76, O 3.29;Measured value:
C 81.38, H 9.51, N 5.79, O 3.31.
Comparative example 3
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel
250ml four-hole boiling flasks in, add 9.24 grams of (33mmol) 2,6- di-t-butyl -4- (3-
Mercaptopropyi) phenol, 3.07 grams of (37mmol) formaldehyde, 11.71 grams (45mmol)
N, N'- diphenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL benzene, rapid stirring, at 80 DEG C 4h is reacted.
After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography
The shielding phenol product of structure shown in isolated title.
Characterization of The Products data are as follows:
1H NMR (300MHz, CDCl3):δ 1.40 (18H), 1.99 (1H), 2.61-2.80
(6H), 4.63 (2H), 5.32 (1H), 6.97-7.02 (12H), 7.26 (4H),
7.55(1H);
13C NMR (75MHz, CDCl3):δ 28.7,31.1,34.3,35.7,54.1,
117.1,119.4,123.3,124.8,129.2,131.8,136.0,142.8,144.9,
146.1,151.9;
C36H44N2OS calculated values C 78.22, H 8.02, N 5.07, O 2.89, S 5.80;
Measured value:C 78.27, H 7.96, N 4.98, O 2.92, S 5.83.
Comparative example 4~7
The composition of the comparative example 4~7 of antioxidant is shown in Table 1.
Table 1
The embodiment 19~28 of industrial lubricant and the formula composition of comparative example 8~14 are shown in Table
2、3.Each component in table is added to scale in mediation container, in 45 DEG C of heating
Stirring 2 hours, prepares obtain industrial lubrication fluid composition respectively.
Some lube oil additives for specifically being used are as follows:
Extreme pressure anti-wear additives:Sulfide isobutene, trade names T321;Thiophosphate is nitrogenous
Derivative, trade names T305;The multiple ester amine salt of thiophosphate, T307.
Metal deactivator:2,5- double (octyl group two is thio) thiadiazoles, trade names T561.
Antirust agent:Heptadecenyl imidazolidene succinate, trade names T703;Ten
Dialkylene succinic acid, trade names T746.
Lube base oil:I class base oil 150SN, II base oil 200N.
Table 2
Table 3
PDSC tests, coking simulated test, four-ball test, high-frequency reciprocating friction test, copper sheet are rotten
The test result of corrosion test and corrosion test is as shown in table 4.
Table 4
From table 4, it can be seen that industrial lubrication fluid composition of the present invention has excellent high-temperature oxidation resistance
Can, detergent-dispersant performance energy and extreme pressure property, preferable abrasion-resistance and relatively low coefficient of friction and
Excellent corrosion resistance and anti-corrosion ability.
Claims (10)
1. a kind of industrial lubrication fluid composition, including shielding phenolic compounds, extreme pressure anti-wear additives, metal
Passivator, antirust agent and major amount of lube base oil, the structure of the shielding phenolic compounds is:
In logical formula (I), each group R is same to each other or different to each other, and is each independently selected from hydrogen, C1-300
Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn are
300-3000's is polyolefin-based), the group shown in logical formula (II) and the group shown in logical formula (III),
On condition that at least one group R is the group shown in logical formula (II);Each group R' is mutually the same or not
Together, hydrogen and C are each independently selected from1-20Straight or branched alkyl (is preferably each independently selected from hydrogen
And C1-4Straight or branched alkyl),
In aforementioned each logical formula (II), (III) and (IV), each group L is same to each other or different to each other, respectively
From being independently groupWherein group R " is selected from hydrogen, C1-20Alkyl (preferred C1-20
Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain or
Branched alkyl and C3-10Straight or branched miscellaneous alkyl;Each group R2It is same to each other or different to each other, each solely
On the spot it is selected from hydrogen, C1-20Group and logical formula (V) shown in straight or branched alkyl, logical formula (IV)
Shown group (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and logical formula (IV)
Shown group);Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20Directly
Chain or branched alkyl (are preferably each independently selected from hydrogen and C1-10Straight or branched alkyl);Each group
RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly
Chain or branched alkyl epoxide (are preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and C1-10
Straight or branched alkyl epoxide, is more preferably in cyclic groupThe contraposition of upper nitrogen-atoms);y
It is 0 to 3 integer (preferably 0 or 1);Z is 0 to 3 integer (preferably 0 or 1);N is 1
To 8 integer (preferably 1 or 2);N' is 0 to 7 integer (preferably 0,1 or 2), on condition that
N'+n≤8 (preferred n'+n=1 or n'+n=2);Each group RdIt is same to each other or different to each other, independently of one another
Selected from the group (preferred hydrogen) shown in hydrogen and logical formula (V);Each cyclic groupIt is mutually the same
Or it is different, phenyl ring and naphthalene nucleus (preferred phenyl ring) are each independently selected from, wherein two adjacent ring groups
GroupOptionally formed by the S atom for adding and the N atoms for bridging the two rings each other
Phenthazine ring, and/or, two adjacent cyclic groupsEach other optionally by additional group(wherein group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl)
And C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen and C1-10Straight or branched alkyl) and bridge joint
The N atoms of the two rings and form 9,10- acridan rings,
In logical formula (V), each group R is same to each other or different to each other, and is each independently selected from hydrogen, C1-300
Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn are 300-3000
It is polyolefin-based), the group shown in logical formula (II) and the group shown in logical formula (III) (preferably each solely
On the spot selected from hydrogen and C1-300Straight or branched alkyl);Each group R' is same to each other or different to each other, each solely
On the spot selected from hydrogen and C1-20Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-4Straight chain
Or branched alkyl);Group L is groupWherein group R " is selected from hydrogen, C1-20Hydrocarbon
Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, be preferably selected from hydrogen,
C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl;A is 0 or 1, and two bases
R and group-(S) of groupa- L- occupies respectively three positions of residue on phenyl ring,
Wherein, the straight or branched miscellaneous alkyl is selected from inside straight or branched alkyl molecular structure
Individual or multiple (such as 1 to 4,1 to 3,1 to 2 or 1) group-CH2- quilt
Selected from-O- ,-S- and-NR'-, (R' is H or C1-4Straight or branched alkyl) one of substituting group
One or more inside the group for directly substituting and obtaining and straight or branched alkyl molecular structure
(such as 1 to 3,1 to 2 or 1) group-CH<By substituting group-N<Directly replace
Generation and obtain group, wherein the shielding phenolic compounds in its whole molecular structure at least one
Group RdIt is hydrogen.
2. according to the industrial lubrication fluid composition described in claim 1, it is characterised in that described
Mixture of the shielding phenolic compounds selected from following particular compound or its arbitrary proportion:
3. a kind of industrial lubrication fluid composition, including shielding phenolic compounds, extreme pressure anti-wear additives, metal
Passivator, antirust agent and major amount of lube base oil, the manufacturer of the shielding phenolic compounds
Method includes making phenolic compounds and the amines shown in formula (Y) shown in logical formula (X) in formula
(Z) first step reacted in the presence of the aldehyde compound (preferred formaldehyde) shown in, optionally
Also include making the product of the first step react with vulcanizing agent (preferred sulphur) and/or and formula
(Z) additional step of aldehyde compound (preferred formaldehyde) reaction shown in,
In logical formula (X), each group R0It is same to each other or different to each other, is each independently selected from hydrogen ,-SH
And C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn
For the polyolefin-based of 300-3000), on condition that at least one group R0It is-SH;Each group R' is each other
It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl is (preferably each independent
Ground is selected from hydrogen and C1-4Straight or branched alkyl),
In formula (Y), group R'2Selected from hydrogen, C1-20Straight or branched alkyl and groupEach group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20
Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-10Straight or branched alkyl);Each base
Group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20
Straight or branched alkyl epoxide (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and
C1-10Straight or branched alkyl epoxide, is more preferably in cyclic groupThe contraposition of upper nitrogen-atoms);
Y is 0 to 3 integer (preferably 0 or 1);Z is 0 to 3 integer (preferably 0 or 1);n1
For 1 to 8 integer (preferably 1 or 2);Each cyclic groupIt is same to each other or different to each other, respectively
From independently selected from phenyl ring and naphthalene nucleus (preferred phenyl ring),
In formula (Z), group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkane
Base) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight or branched alkyl and C3-10
Straight or branched miscellaneous alkyl,
Wherein, the straight or branched miscellaneous alkyl is selected from inside straight or branched alkyl molecular structure
Individual or multiple (such as 1 to 4,1 to 3,1 to 2 or 1) group-CH2- quilt
Selected from-O- ,-S- and-NR'-, (R' is H or C1-4Straight or branched alkyl) one of substituting group
One or more inside the group for directly substituting and obtaining and straight or branched alkyl molecular structure
(such as 1 to 3,1 to 2 or 1) group-CH<By substituting group-N<Directly replace
Generation and obtain group.
4. according to the industrial lubrication fluid composition described in claim 3, it is characterised in that described
In first step, the phenolic compounds shown in the logical formula (X) and the amine shown in the formula (Y)
The mol ratio of compound is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, the formula
(X) phenolic compounds shown in is 1 with the mol ratio of the aldehyde compound shown in the formula (Z):0.1-10,
It is preferred that 1:0.5-5.0, more preferably 1:0.8-2.0, in the additional step, formula (Y) institute
The amines for showing is 1 with the mol ratio of the vulcanizing agent:1-10, preferably 1:1.2-6.0, more preferably
1:1.5-3.0, the amines shown in the formula (Y) is closed with the hydroformylation shown in the formula (Z)
The mol ratio of thing is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
5. according to the industrial lubrication fluid composition described in one of claim 1-4, it is characterised in that
The shielding phenolic compounds accounts for the 0.001-30% of the industrial lubricant composition total weight;
The extreme pressure anti-wear additives selected from olefine sulfide, phosphate derivative, phosphorothioate derivative,
One or more in dialkyl dithiocarbamate and dialkyl dithiophosphate, accounts for described
The 0.01%-10% of industrial lubrication fluid composition gross mass;
The metal deactivator accounts for the work selected from benzotriazole derivative and/or thiadiazoles derivative
The 0.01%-1% of industry lubricant oil composite gross mass;
The antirust agent is in sulfonate, alkyl imidazolidine derivatives and alkenyl succinic acid derivative
One or more, account for the 0.001%-10% of the industrial lubrication fluid composition gross mass;
The lube base oil is in API I, II, III, IV and V class lubricating oil base oils
One or more.
6. according to the industrial lubrication fluid composition described in one of claim 1-4, it is characterised in that
Both the extreme pressure anti-wear additives are selected from the combination of olefine sulfide and phosphorothioate derivative, in the combination
Between mass ratio be 0.01:1~100:1;The metal deactivator is selected from thiadiazoles derivative;Institute
Antirust agent is stated selected from alkyl imidazoline alkenyl succinate and/or alkenyl succinic acid.
7. according to the industrial lubrication fluid composition described in one of claim 1-4, it is characterised in that
The shielding phenolic compounds accounts for the 0.05%-20% of the industrial lubricant composition total weight;Institute
State the 0.05%-8% that extreme pressure anti-wear additives account for the industrial lubrication fluid composition gross mass;The metal subtracts
Agent living accounts for the 0.02%-0.5% of the industrial lubrication fluid composition gross mass;The antirust agent accounts for described
The 0.005%-5% of industrial lubrication fluid composition gross mass.
8. according to the industrial lubrication fluid composition described in one of claim 1-4, it is characterised in that
The shielding phenolic compounds accounts for the 0.1%-10% of the industrial lubricant composition total weight;It is described
Extreme pressure anti-wear additives account for the 0.1%-5% of the industrial lubrication fluid composition gross mass;The metal deactivator
Account for the 0.03%-0.3% of the industrial lubrication fluid composition gross mass;The antirust agent accounts for the industry
The 0.01%-1% of lubricant oil composite gross mass.
9. according to the industrial lubrication fluid composition described in one of claim 1-4, it is characterised in that
In the industrial lubrication fluid composition add antioxidant, detersive, dispersant, pour-point depressant,
One or more in viscosity index improver, friction improver, anti emulsifier and anti-foaming agent.
10. the manufacture method of the industrial lubrication fluid composition described in one of claim 1-4, including
Make the shielding phenol, extreme pressure anti-wear additives, metal deactivator, antirust agent and the lube base oil
The step of mixing.
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