GB756981A - Preparation of formylated fatty compounds and corresponding hydroxylated compounds, including isomers thereof - Google Patents
Preparation of formylated fatty compounds and corresponding hydroxylated compounds, including isomers thereofInfo
- Publication number
- GB756981A GB756981A GB6818/54A GB681854A GB756981A GB 756981 A GB756981 A GB 756981A GB 6818/54 A GB6818/54 A GB 6818/54A GB 681854 A GB681854 A GB 681854A GB 756981 A GB756981 A GB 756981A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- compounds
- formylated
- catalyst
- per cent
- 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
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/01—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Formylated fatty compounds are prepared by reacting one or more fatty compounds with commercial formic acid containing 5 to 15 per cent by weight of water at a temperature between about 70 DEG C. and the normal boiling point of the reaction mixture in the presence of added strong mineral acid as catalyst, sufficient of the formic acid being present to allow its addition to a double bond of the fatty compound. The formylated products may be hydrolysed to the corresponding hydroxylated compounds. The starting materials are those defined in the parent Specification. Sulphuric acid is preferred as catalyst; perchloric acid may also be used. In examples: (1) oleic acid is refluxed with 90 per cent formic acid using sulphuric acid as catalyst and the resulting formoxy stearic acid is hydrolysed to monohydroxy-stearic acid; (4) oleic acid containing linoleic acid is formoxylated with 90 per cent formic acid in a number of experiments in which the catalytic effects of sulphuric acid and perchloric acid are compared.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US756981XA | 1953-03-13 | 1953-03-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB756981A true GB756981A (en) | 1956-09-12 |
Family
ID=22127426
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6818/54A Expired GB756981A (en) | 1953-03-13 | 1954-03-09 | Preparation of formylated fatty compounds and corresponding hydroxylated compounds, including isomers thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB756981A (en) |
-
1954
- 1954-03-09 GB GB6818/54A patent/GB756981A/en not_active Expired
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