GB886460A - Improvements in or relating to the manufacture of aromatic ethers - Google Patents
Improvements in or relating to the manufacture of aromatic ethersInfo
- Publication number
- GB886460A GB886460A GB23698/60A GB2369860A GB886460A GB 886460 A GB886460 A GB 886460A GB 23698/60 A GB23698/60 A GB 23698/60A GB 2369860 A GB2369860 A GB 2369860A GB 886460 A GB886460 A GB 886460A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- alkenyl
- ethers
- catalyst
- butenyl
- 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
- 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
-
- 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
- C07D303/28—Ethers with hydroxy compounds containing oxirane rings
-
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
Abstract
Epoxy resins which have been prepared by reacting a phenol with at least two moles of a conjugated diene in the presence of an alkane sulphonic acid, tin tetrachloride or boron trifluoride or a complex thereof as catalyst and then epoxidizing the resulting alkenyl ether of the alkenyl phenol to give a polyepoxide containing at least one epoxyalkyl and at least one epoxyalkoxy group bound to an aromatic nucleus, are cured with phthalic anhydride. Examples describe the curing of epoxidized butenyl phenol butenyl ethers. Specifications 828,364 and 841,589 are referred to.ALSO:A process for the manufacture of alkenyl or cyclo-alkenyl ethers of alkenyl or cyclo-alkenyl phenols comprises reacting 1 mol of a phenol with at least 2 mols of a conjugated diene in the presence of an alkane sulphonic acid, in tetrachloride or boron trifluoride or a complex thereof as catalyst. The reaction preferably takes place at 0 DEG C.-30 DEG C. using 3-8 mols of diene and boron trifluoride diethyl etherate as catalyst. Lists of suitable phenols and dienes are given. Examples describe the reaction of butadiene with phenol, m-cresol, resorcinol, b -naphthol and bis-(p-hydroxyphenyl)-dimethylmethane and of isoprene and dicyclopentadiene with phenol. A mixture of products are obtained; using phenol and butadiene, for example, butenyloxy butenylbenzene, bis (butenyloxy - phenyl)-butane and (butenyloxyphenyl)-(butenyl-oxy-butenylphenyl) butane are obtained. Epoxides containing at least one epoxyalkyl and at least one epoxyalkoxy group bound to an aromatic nucleus are obtained by epoxidising the unsaturated phenol ethers, for example, with an organic per acid. Specifications 828,364 and 841,589 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH886460X | 1959-07-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB886460A true GB886460A (en) | 1962-01-10 |
Family
ID=4545311
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23698/60A Expired GB886460A (en) | 1959-07-06 | 1960-07-06 | Improvements in or relating to the manufacture of aromatic ethers |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE592617A (en) |
GB (1) | GB886460A (en) |
-
0
- BE BE592617D patent/BE592617A/xx unknown
-
1960
- 1960-07-06 GB GB23698/60A patent/GB886460A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE592617A (en) |
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