US20040029744A1

US20040029744A1 - Cyclic thioamides as additives for lubricating oils

Info

Publication number: US20040029744A1
Application number: US10/636,185
Authority: US
Inventors: Ravindranath Mukkamala
Original assignee: Individual
Current assignee: Individual
Priority date: 2002-08-07
Filing date: 2003-08-07
Publication date: 2004-02-12
Also published as: EP1394239A1; JP2004162028A

Abstract

A composition comprising: (a) from 0.1% to 20% of at least one cyclic thioamide of formula I:

wherein X is CR⁵R⁶, CR⁵R⁶NR⁷or CR⁵R⁶CR⁸R⁹; R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹are independently hydrogen, alkyl, alkenyl, aryl or aralkyl; or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; and (b) a lubricating oil.

Description

BACKGROUND

This invention relates generally to cyclic thioamides useful as additives for lubricating oils.

Zinc dialkyldithiophosphates (ZDDP) are widely used as lubricant additives. The principal disadvantages of these compounds are that an ash residue is produced by the zinc as the additive is consumed, and that phosphorus is known to affect the efficiency of catalytic converters in motor vehicles, thereby causing emissions problems. Cyclic compounds useful as lubricant additives are disclosed in U.S. Pat. No. 6,187,722. However, the compounds disclosed therein are imidazolidinethiones which are not within the scope of the present invention.

The problem addressed by this invention is to find additional non-metallic, non-phosphorus-containing oil-soluble additives for lubricating oils.

STATEMENT OF INVENTION

The present invention is directed to a composition comprising:

(a) from 0.1% to 20% of at least one cyclic thioamide of formula I:

wherein X is CR ⁵R⁶, CR⁵R⁶NR⁷or CR⁵R⁶CR⁸R⁹; R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹are independently hydrogen, alkyl, alkenyl, aryl or aralkyl; or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; and

(b) a lubricating oil.

The present invention is further directed to a method for improving the anti-wear characteristics of a lubricating oil by adding from 0.1% to 20% of a compound of formula I.

The present invention is further directed to a lubricating oil composition containing the reaction product of a compound of formula (I) with an imine; an unsaturated carboxylic acid or ester; an isocyanate or isothiocyanate; or an alkyl, alkenyl or aralkyl group bearing a leaving group; and to the aforementioned reaction products.

DETAILED DESCRIPTION

All percentages are weight percentages based on the entire composition described, unless specified otherwise. An “alkyl” group is a saturated hydrocarbyl group having from one to twenty-two carbon atoms in a linear, branched or cyclic arrangement, and having from 0 to 2 oxygen, nitrogen or sulfur atoms. Substitution on alkyl groups of one or more halo, hydroxy, alkoxy, alkanoyl or amido groups is permitted; alkoxy, alkanoyl and amido groups may in turn be substituted by one or more halo substituents. In one preferred embodiment, alkyl groups contain from two to twelve carbon atoms and from 0 to 1 oxygen, nitrogen or sulfur atoms; in another preferred embodiment, alkyl groups contain from 4 to 22 carbon atoms; in another preferred embodiment, alkyl groups contain no heteroatoms. An “alkenyl” group is an “alkyl” group in which at least one carbon-carbon single bond has been replaced with a double bond. An “aryl” group is a substituent derived from an aromatic compound, including heterocyclic aromatic compounds having heteroatoms chosen from among nitrogen, oxygen and sulfur. An aryl group has a total of from five to twenty ring atoms, and has one or more rings which are separate or fused. Substitution on aryl groups of one or more halo, alkyl, alkenyl, hydroxy, alkoxy, alkanoyl or amido groups is permitted, with substitution by one or more halo groups being possible on alkyl, alkenyl, alkoxy, alkanoyl or amido groups. An “aralkyl” group is an “alkyl” group substituted by an “aryl” group. A “lubricating oil” is a natural or synthetic oil, or a mixture thereof, having suitable viscosity for use as a lubricant, e.g., as crankcase oil in an internal combustion engine, automatic transmission fluid, turbine lubricant, gear lubricant, compressor lubricant, metal-working lubricant, hydraulic fluid, etc. [0010]
Preferably, at least one of R[0011] ¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹is alkyl, alkenyl, aryl or aralkyl or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; more preferably at least two of R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹are alkyl, alkenyl, aryl or aralkyl. In one embodiment of the invention at least one of R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹is aryl, aralkyl, C₄-C₂₂alkyl or C₄-C₂₂alkenyl; more preferably at least one of R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹is C₄-C₂₂alkyl or C₄-C₂₂alkenyl; and most preferably at least one of R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹is C₆-C₂₂alkyl. The composition of the present invention includes at least one compound of formula (I). In one embodiment of the invention, the composition contains at least two compounds of formula (I), and more preferably contains at least three compounds of formula (I).
In one embodiment of the invention, R[0012] ¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring, preferably a C₅-C₈alkyl or alkenyl ring, most preferably a C₅-C₆alkyl ring. In this embodiment, either or both pairs of substituents, R¹and R², or R³and R⁴, become a difunctional alkyl or alkenyl group linked to the cyclic thioamide ring carbon to form an alkyl or alkenyl ring, resulting in a mono- or di-spiro-compound. For example, when X is CH₂; and R¹and R², and R³and R⁴combine with a ring carbon atom to form a C₆alkyl ring, the following structure results:
In one embodiment of the invention, X is CR[0013] ⁵R⁶, and the compound of formula (I) can be represented by formula (II)
Preferably, at least one of R[0014] ¹, R², R³, R⁴, R⁵and R⁶is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring. In a preferred embodiment of the invention, R⁴is R¹⁰NH, and R¹⁰is alkyl, alkenyl, aryl or aralkyl. The compound of this embodiment can be prepared from an alkyl nitrile, a ketone bearing a leaving group at the α-position, and an amine, in a three-step process, as shown below in Scheme 1 for the embodiment in which R⁵and R⁶are hydrogen:
wherein Z represents a suitable leaving group, including, but not limited to iodide, bromide, chloride, tosylate, mesylate or triflate. Preferably, R[0015] ³is alkyl, alkenyl, aryl or aralkyl. Preferably, R¹, R²and R³contain no amine nitrogen atoms. Preferably, at least one of R¹, R², R³and R¹⁰is aryl, aralkyl, C₄-C₂₂alkyl or C₄-C₂₂alkenyl; more preferably C₆-C₂₂alkyl or C₆-C₂₂alkenyl; and most preferably C₁₀-C₂₂alkyl. Use of a more highly substituted ketone starting material will result in a product in which one or both of R⁵and R⁶are not hydrogen.
In one embodiment of the invention, a compound of formula (I) in which X is CH[0016] ₂is prepared from a 1,2-halohydrin, an alkyl nitrile and a sulfide salt, in a two-step process, as shown below in Scheme 2:
wherein Z represents a suitable leaving group, including, but not limited to iodide, bromide, chloride, tosylate, mesylate or triflate. The process can also be performed with substituted starting material to produce a compound in which X is CR[0017] ⁵R⁶, and R⁵and R⁶are not hydrogen.
In another embodiment of the invention, X is CR[0018] ⁵R⁶CR⁸R⁹and the compound of formula (I) can be represented by formula (III)
Preferably, at least one of R[0019] ¹, R², R³, R⁴, R⁵, R⁶, R⁸and R⁹is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring. In a preferred embodiment of the invention, R⁴is R¹⁰NH, and R¹⁰is alkyl, alkenyl, aryl or aralkyl. Preferably, R³is alkyl, alkenyl, aryl or aralkyl. Preferably, R³contains no amine nitrogen atoms. Preferably, at least one of R³and R⁴is aryl, aralkyl, C₄-C₂₂alkyl or C₄-C₂₂alkenyl; more preferably C₆-C₂₂alkyl or alkenyl; and most preferably C₁₀-C₂₂alkyl. In one embodiment of the invention, R¹, R², R⁵, R⁶, R⁸and R⁹are hydrogen, and the compound of formula (III) is prepared according to the following two-step process
This process also may be performed with various R groups on the starting material to give substituted versions of the product in which some or all of R[0020] ¹, R², R⁵, R⁶, R⁸and R⁹are not hydrogen. The process also is capable of producing the five-membered analog of the product, i.e., X is CR⁵R⁶, with or without substituents on the ring carbons. This is illustrated below in Scheme 4 for the embodiment in which R¹, R², R⁵and R⁶are hydrogen:
In another embodiment of the invention, X is CR[0021] ⁵R⁶NR⁷and the compound of formula (I) can be represented by formula (IV)
Preferably, at least one of R[0022] ¹, R², R³, R⁴, R⁵, R⁶and R⁷is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring. In a preferred embodiment, R¹, R², R⁵, R⁶and R⁷are hydrogen, and the compound of formula (IV) is prepared according to the following two-step process
This process also may be performed with various R groups on the starting material, or with subsequent alkylation on the amine nitrogen, to give substituted versions of the product in which some or all of R[0023] ¹, R², R⁵, R⁶and R⁷are not hydrogen. Preferably, at least one of R³and R⁴is alkyl, alkenyl, aryl or aralkyl; more preferably at least one of R³and R⁴is aryl, aralkyl, C₄-C₂₂alkyl or C₄-C₂₂alkenyl; more preferably C₆-C₂₂alkyl or C₆-C₂₂alkenyl; and most preferably C₁₀-C₂₂alkyl. Preferably, R³and R⁴contain no amine nitrogen atoms.
In a preferred embodiment of the invention, the thioamide group or an amine group of the compound of formula (I) is further functionalized by reaction with imines of formula R[0024] ¹¹N═CR¹²R¹³; unsaturated carboxylic esters of formula CHR¹⁴═CR¹⁵COOR¹⁶; isocyanates, R¹⁸NCO, or isothiocyanates, R¹⁸NCS; or R¹⁷Y; wherein R¹², R¹³and R¹⁶independently are hydrogen, alkyl, alkenyl, aryl or aralkyl; R¹⁷is alkyl, alkenyl or aralkyl; R¹⁴and R¹⁵independently are hydrogen or C₁-C₄alkyl; R¹¹and R¹⁸independently are alkyl, alkenyl, aryl or aralkyl; and Y is a suitable leaving group capable of being displaced by the nitrogen or the sulfur of a thioamide group, or by a primary or secondary amine nitrogen. Suitable leaving groups include, e.g., iodide, bromide, chloride, tosylate, mesylate or triflate. Functionalization of the thioamide group can occur on the thioamide nitrogen or the thioamide sulfur, provided of course that the thioamide nitrogen bears at least one hydrogen. The product also can be a mixture of the compound functionalized on the nitrogen and the one functionalized on the sulfur. In compounds also having a primary or secondary amino group, functionalization also may occur solely or partially on the amino group.
Preferably, R[0025] ¹⁴and R¹⁵independently are hydrogen or methyl. Preferably, the compound of formula CHR¹⁴═CR¹⁵COOR¹⁶is an alkyl or aralkyl acrylate having R¹⁴=R¹⁵=H and R¹⁶=alkyl or aralkyl; or a methacrylate ester having R¹⁴=H and R¹⁵=CH₃; or a crotonate ester having R¹⁵=H and R¹⁴=CH₃. Preferably, R¹⁴is hydrogen. Preferably, R¹⁶is alkyl or aralkyl, most preferably C₄-C₂₂alkyl. Preferably, R¹⁸is aryl, alkyl or aralkyl, most preferably C₈-C₂₂alkyl. Preferably, R¹¹is C₁₂-C₂₂alkyl. In one embodiment, R¹¹is derived from an unsubstituted C₁₆-C₂₂alkyl amine, R¹¹NH₂, preferably one which is an oil-soluble amine. In one embodiment, the alkyl amine is a tertiary alkyl primary amine, i.e., a primary amine in which the alkyl group is attached to the amino group through a tertiary carbon. Examples of commercially available tertiary alkyl primary amines are the Primene™ amines available from Rohm and Haas Company, Philadelphia, Pa. Preferably, R¹²and R¹³independently are alkyl or hydrogen. In a preferred embodiment of the invention, R¹¹N═CR¹²R¹³is a formaldehyde imine, R¹¹N=CH₂. Preferably, R¹⁷is C₄-C₂₂alkyl, C₄-C₂₂alkenyl or aralkyl; more preferably C₆-C₂₂alkyl or C₆-C₂₂alkenyl; and most preferably C₈-C₂₂alkyl.
As an example, the reaction of the compound of formula (II) with an imine and an acrylate is illustrated below in Scheme 6. [0026]
The compound resulting from functionalization of the thioamide group in the compound of formula (II) can be represented by formula (V). [0027]
wherein bonds a and b are single or double bonds, provided that one of a and b is a single bond and the other is a double bond; one of B[0028] ¹and B²is —CR¹⁴H—CR¹⁵H—COOR¹⁶, —CR¹²R¹³NHR¹¹, —C(O)NHR¹⁸, —C(S)NHR¹⁸or R¹⁷, and the other is absent. When B¹is present, bond “b” is a double bond; and when B²is present, bond “a” is a double bond. An analogous structure exists for the compound resulting from functionalization of the compound of formula (III), in which functionalization also occurs on the thioamide nitrogen or sulfur, as shown in formula (VI).
The compound resulting from functionalization of the thioamide group and/or a secondary amino group in the compound of formula (IV) can be represented by formula (VII). [0029]
wherein B[0030] ³represents R⁷, —CR¹⁴H—CR¹⁵H—COOR¹⁶, —CR¹²R¹³NHR¹¹, —C(O)NHR¹⁸, —C(S)NHR¹⁸or R¹⁷. If R⁷in formula (IV) is not hydrogen, then functionalization at the NR⁷amino group would not occur, and B³would simply be R⁷. Other primary or secondary amino groups in formulas (II), (III) or (IV) can be functionalized in this way, e.g., when R⁴is R¹⁰NH, the R¹⁰NH amino group can be functionalized.
Preferably, the compound(s) of formula (I) is present in a lubricating oil in a total amount of at least 0.2%, more preferably at least 0.3%, and most preferably at least 0.4%. Preferably, the compound(s) of formula (I) is present in a lubricating oil in a total amount no greater than 10%, more preferably no greater than 5%, and most preferably no greater than 2%. Preferably, the compounds are soluble at the aforementioned levels. [0031]
Optionally, other additives typically used in lubricating oils are present in the composition. Such additives include, but are not limited to, other anti-wear additives, anti-corrosion additives, dispersants, detergents, antioxidants, antifoamants, friction modifiers, seal swell agents, demulsifiers, viscosity index improvers and pour point depressants. Other anti-wear additives that can be used in combination with the compound of formula (I) include the commercial products known as ZDDP, which are zinc dialkyldithiophosphates. In addition to improving the anti-wear characteristics of lubricating oils, the compound of formula (I) typically also improves anti-corrosion characteristics and functions as an anti-oxidant. [0032]

Claims

1. A composition comprising:

(a) from 0.1% to 20% of at least one cyclic thioamide of formula I:

wherein X is CR⁵R⁶, CR⁵R⁶NR⁷or CR⁵R⁶CR⁸R⁹; R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹are independently hydrogen, alkyl, alkenyl, aryl or aralkyl; or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; and

(b) a lubricating oil.

2. The composition of claim 1 in which X is CR⁵R⁶, and at least one of R¹, R², R³, R⁴, R⁵and R⁶is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring.

3. The composition of claim 2 in which R⁴is R¹⁰NH, and R¹⁰is alkyl, alkenyl, aryl or aralkyl.

4. The composition of claim 1 in which X is CR⁵R⁶CR⁸R⁹, and at least one of R¹, R², R³, R⁴, R⁵, R⁶, R⁸and R⁹is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring.

5. The composition of claim 4 in which R⁴is R¹⁰NH, and R¹⁰is alkyl, alkenyl, aryl or aralkyl.

6. The composition of claim 1 in which X is CR⁵R⁶NR⁷, and at least one of R¹, R², R³, R⁴, R⁵and R⁶is alkyl, alkenyl, aryl or aralkyl, or R¹and R², or R³and R⁴, combine with the carbon atom to which they are attached to form a C₅-C₈alkyl or alkenyl ring.

7. The composition of claim 6 in which R⁷is hydrogen, and at least one of R³and R⁴is alkyl, alkenyl, aryl or aralkyl.

8. The composition of claim 1 in which at least one of R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸and R⁹is aryl, aralkyl, C₄-C₂₂alkyl or C₄-C₂₂alkenyl.

9. The composition of claim 1 which comprises at least two cyclic thioamide compounds of formula (I).

10. The method of claim 9 in which said at least two cyclic thioamide compounds are present in a total amount from 0.2% to 5%.