GB1082104A - Polyepoxides - Google Patents
PolyepoxidesInfo
- Publication number
- GB1082104A GB1082104A GB4060565A GB4060565A GB1082104A GB 1082104 A GB1082104 A GB 1082104A GB 4060565 A GB4060565 A GB 4060565A GB 4060565 A GB4060565 A GB 4060565A GB 1082104 A GB1082104 A GB 1082104A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- hydrocarbon
- aryl
- carbon atoms
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/22—Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/16—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/34—Compounds containing oxirane rings with hydrocarbon radicals, substituted by sulphur, selenium or tellurium atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/30—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
- C08G59/302—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Epoxy resins are prepared by treating an epoxide coupling reagent and, optionally, an epoxide polymerizing catalyst with novel polythioepoxides, preferably of formula <FORM:1082104/C3/1> where n is an integer of 2 or more; R is an n-valent organic radical, such that at least 2 of the sulphur atoms are no more than 6 carbon atoms away from each other or from a negative activating group; R is a hydrocarbon, hydrocarbon-ether or hydrocarbon-ester chain including at least 2 carbon atoms, which hydrocarbon chain may comprise a 5- or 6-membered carbocyclic ring, or an alkyl, aryl or halogen substituted derivative thereof; R2 and R3 are hydrogen, alkyl or halogen; R4, when not connected to R1, is hydrogen, halogen, alkyl, haloalkyl, aryl, haloaryl, alkyaryl or haloalkaryl, and, when connected to R1, is a hydrocarbon chain of 2 or 3 carbon atoms or an alkyl, aryl or halogen substituted derivative thereof, are prepared by reacting a polymercaptan R(SH)n with an olefinically unsaturated epoxide containing at least one vicinal epoxide group separated from an olefin group by at least one carbon, the olefin group being located in a 5 or 6-membered carbon ring or in a terminal position in an aliphatic hydrocarbon chain, the reaction product not containing the radical -S-CH2-S-. Specified negative activating groups are -C(O)O-, -OH, -S-, -O- and -CO-. Examples prepare resins from reaction products of 1,4-butanedithiol and various esters of polyhydric compounds with mercaptoacetic and b -mercaptopropionic acids with alkyl glycidyl ether, the glycidyl ether of 2-alkyl-phenol, vinyl-3,4-epoxycyclohexane, limonene monoxide or glycidyl acrylate. The polythioepoxides may be prepared, at least in part, in situ in the presence of the epoxide coupling agent. Examples use methylbicyclo-2,2,1-hept-5-ene-2,3-dicarboxylic anhydride, phthalic anhydride or maleic anhydride as coupling agents, and 2,4,6-tris(dimethylaminomethyl)phenol as catalyst, when used. The mercaptoacetate of an allyl alcohol-styrene copolymer is prepared in Example 8 by conventional esterification and the mercaptoacetate of a phenol-formaldehyde resin similarly in Example 14. The novel polythioepoxides described above may be used to stabilize vinyl chloride resin compositions.ALSO:Novel polythio - group containing polyepoxides, preferably of formula <FORM:1082104/C2/1> where n is an integer of 2 or more; R is an n-valent organic radical, such that at least 2 of the sulphur atoms are no more than 6 carbon atoms away from each other or from a negative activating group; R1 is a hydrocarbon, hydrocarbon-ether or hydrocarbon-ester chain including at least 2 carbon atoms, which hydrocarbon chain may comprise a 5- or 6-membered carbocyclic ring, or an alkyl, aryl or halogen substituted derivative thereof; R2 and R3 are hydrogen, alkyl or halogen; R4, when not connected to R1 is hydrogen, halogen, alkyl, haloalkyl, aryl, haloaryl, alkaryl or haloalkaryl, and, when connected to R1 is a hydrocarbon chain of 2 or 3 carbon atoms or an alkyl, aryl or halogen substituted derivative thereof, are prepared by reacting a polymercaptan R(SH)n with an olefinically unsaturated epoxide containing at least one vicinal epoxide group separated from an olefin group by at least one carbon, the olefin group being located in a 5- or 6-membered carbon ring or in a terminal position in an aliphatic hydrocarbon chain, the reaction product not containing the radical -S-CH2-S-. Specified negative activating groups are -C(O)O-, -OH, -S-, -O-and -CO-. Examples react 1,4-butanedithiol and various esters of polyhydric compounds with mercaptoacetic and b -mercaptopropionic acids with allyl glycidyl ether, the glycidyl ether of 2-allylphenol, vinyl-3,4-epoxycyclohexane, limonene monoxide, or glycidyl acrylate. Conventional esterification is used to prepare, as starting materials, the completely esterified mercaptoacetate of triethylene glycol, 1,4 - butanediol, 1,1,1 - trimethylolpropane, glycerol, 1,1,1 - trimethylolethane, pentaery - thritol, hydroxylated castor oil and bisphenol A, the b - mercaptopropionate of 1,1,1 - trimethylolpropane, mixed esters of pentaerythritol with mercaptoacetic acid and soya bean oil acids and of 1,1,1-trimethylolpropane with mercaptoacetic and dimerized soya bean oil acids, and the mercaptoethanol ester of adipic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4060565A GB1082104A (en) | 1965-09-23 | 1965-09-23 | Polyepoxides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4060565A GB1082104A (en) | 1965-09-23 | 1965-09-23 | Polyepoxides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1082104A true GB1082104A (en) | 1967-09-06 |
Family
ID=10415719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4060565A Expired GB1082104A (en) | 1965-09-23 | 1965-09-23 | Polyepoxides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1082104A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120071587A1 (en) * | 2009-03-16 | 2012-03-22 | Astrium Sas | Use of curable resins containing a prepolymer based on glycidyl (meth)acrylate for making materials for use in space |
CN104262624A (en) * | 2014-09-03 | 2015-01-07 | 浙江大学 | Synthetic method of polyepoxy polymer |
WO2018049302A1 (en) * | 2016-09-12 | 2018-03-15 | Poly6 Technologies | One-pot, high-performance recycling method for polymer waste using renewable polymer synthesis |
CN112794991A (en) * | 2021-02-01 | 2021-05-14 | 南宁珀源能源材料有限公司 | Acrylic acid modified polythiol curing agent and preparation method thereof |
-
1965
- 1965-09-23 GB GB4060565A patent/GB1082104A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120071587A1 (en) * | 2009-03-16 | 2012-03-22 | Astrium Sas | Use of curable resins containing a prepolymer based on glycidyl (meth)acrylate for making materials for use in space |
CN104262624A (en) * | 2014-09-03 | 2015-01-07 | 浙江大学 | Synthetic method of polyepoxy polymer |
WO2018049302A1 (en) * | 2016-09-12 | 2018-03-15 | Poly6 Technologies | One-pot, high-performance recycling method for polymer waste using renewable polymer synthesis |
CN112794991A (en) * | 2021-02-01 | 2021-05-14 | 南宁珀源能源材料有限公司 | Acrylic acid modified polythiol curing agent and preparation method thereof |
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