GB1136688A - Polyallyl esters - Google Patents
Polyallyl estersInfo
- Publication number
- GB1136688A GB1136688A GB1470667A GB1470667A GB1136688A GB 1136688 A GB1136688 A GB 1136688A GB 1470667 A GB1470667 A GB 1470667A GB 1470667 A GB1470667 A GB 1470667A GB 1136688 A GB1136688 A GB 1136688A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- anhydride
- acids
- benzene
- polyallyl
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
1,136,688. Polyallyl esters of benzene polycarboxylic acids. FMC. CORP. 31 March, 1967 [28 April, 1966], No. 14706/67. Heading C2C. Polyallyl esters of a benzene polycarboxylic acid are made by reacting an excess of allyl alcohol with a benzene polycarboxylic acid or anhydride at a temperature of 165-250‹ C. in the absence of a strongly acidic catalyst having a pK below 4, the reaction being carried out in the presence of an esterification catalyst having a pK a above 4 when temperatures below 190‹ C. are used, for a time sufficient to convert at least 90% of the acid to the polyallyl ester. Suitable acids and anhydrides for use as starting materials are, for example, o-phthalic, isophthalic, terephthalic, trimellitic, trimesic, hemimellitic, pyromellitic, mellophanic, pehrritic, benzene-pentacarboxylic and mellitic acids and phthalic anhydride, the inner anhydride of trimellitic acid and pyromellitic acid. Suitable catalysts are, for example, dibutyl tin oxide, tin oxalate and sodium oxalate. Examples are given of the preparation of (a) diallyl phthalate, (b) diallyl isophthalate and (c) triallyl mellitate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US54582766A | 1966-04-28 | 1966-04-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1136688A true GB1136688A (en) | 1968-12-11 |
Family
ID=24177705
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1470667A Expired GB1136688A (en) | 1966-04-28 | 1967-03-31 | Polyallyl esters |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1618412B1 (en) |
GB (1) | GB1136688A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4473702A (en) * | 1979-11-15 | 1984-09-25 | Kureha Kagaku Kogyo Kabushiki Kaisha | Method for producing diallyl ester of aromatic dicarboxylic acid |
PL442176A1 (en) * | 2022-09-01 | 2024-03-04 | Grupa Azoty Zakłady Azotowe Kędzierzyn Spółka Akcyjna | Esters of trimellitic acid and isoprenol, method of their preparation and use of esters of trimellitic acid and isoprenol |
-
1967
- 1967-03-31 GB GB1470667A patent/GB1136688A/en not_active Expired
- 1967-04-28 DE DE1967F0052284 patent/DE1618412B1/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4473702A (en) * | 1979-11-15 | 1984-09-25 | Kureha Kagaku Kogyo Kabushiki Kaisha | Method for producing diallyl ester of aromatic dicarboxylic acid |
PL442176A1 (en) * | 2022-09-01 | 2024-03-04 | Grupa Azoty Zakłady Azotowe Kędzierzyn Spółka Akcyjna | Esters of trimellitic acid and isoprenol, method of their preparation and use of esters of trimellitic acid and isoprenol |
Also Published As
Publication number | Publication date |
---|---|
DE1618412B1 (en) | 1971-12-09 |
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