GB945516A - Process for the preparation of diallylic esters of phthalic acids - Google Patents
Process for the preparation of diallylic esters of phthalic acidsInfo
- Publication number
- GB945516A GB945516A GB961961A GB961961A GB945516A GB 945516 A GB945516 A GB 945516A GB 961961 A GB961961 A GB 961961A GB 961961 A GB961961 A GB 961961A GB 945516 A GB945516 A GB 945516A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloride
- prepared
- sodium carbonate
- diallylic
- anhydride
- 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
- C07C67/10—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond
- C07C67/11—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond being mineral ester groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Diallylic phthalates are prepared by simultaneously reacting a phthalic acid or anhydride thereof with sodium carbonate and an allylic halide in the molar ratio 1:1:2 in the presence of a tertiary amine or a quaternary ammonium salt as catalyst and under substantially anhydrous conditions. In an example a mixture of phthalic anhydride, sodium carbonate, methallyl chloride and triethylamine is refluxed for 15 hours, cooled, filtered to remove sodium chloride, heated to remove unreacted methallyl chloride and finally distilled to give dimethallyl phthalate. Diallyl phthalate and diallyl isophthalate are prepared in further examples the further reactants and catalysts specified being isophthalic acid; allyl chloride; methyldiethylamine, allyltriethylammonium chloride, dodecyltrimethylammonium bromide and cetylbenzyldimethylammonium chloride. Hydroquinone (antioxidant) and 2,21-methylenebis (4-methyl -6-tert-butylphenol) (polymerisation inhibitor) are also present in the reaction mixture in some examples.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1850860A | 1960-03-30 | 1960-03-30 | |
US18514A US3086985A (en) | 1960-03-30 | 1960-03-30 | Preparation of diallylic phthalates |
Publications (1)
Publication Number | Publication Date |
---|---|
GB945516A true GB945516A (en) | 1964-01-02 |
Family
ID=26691190
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB961961A Expired GB945516A (en) | 1960-03-30 | 1961-03-16 | Process for the preparation of diallylic esters of phthalic acids |
Country Status (3)
Country | Link |
---|---|
CH (1) | CH399436A (en) |
ES (1) | ES264693A1 (en) |
GB (1) | GB945516A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0208783A1 (en) * | 1984-12-25 | 1987-01-21 | MITSUI TOATSU CHEMICALS, Inc. | Process for preparing allyl esters |
-
1961
- 1961-02-07 ES ES0264693A patent/ES264693A1/en not_active Expired
- 1961-03-16 GB GB961961A patent/GB945516A/en not_active Expired
- 1961-03-28 CH CH366961A patent/CH399436A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0208783A1 (en) * | 1984-12-25 | 1987-01-21 | MITSUI TOATSU CHEMICALS, Inc. | Process for preparing allyl esters |
EP0208783A4 (en) * | 1984-12-25 | 1987-04-28 | Mitsui Toatsu Chemicals | Process for preparing allyl esters. |
Also Published As
Publication number | Publication date |
---|---|
ES264693A1 (en) | 1961-04-16 |
CH399436A (en) | 1965-09-30 |
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