Dorée et al., 1942 - Google Patents
85. Erucic acid. Preparation of erucic acid. General oxidation reactions. Oxidation with gaseous oxygenDorée et al., 1942
- Document ID
- 11153422165765160592
- Author
- Dorée C
- Pepper A
- Publication year
- Publication venue
- Journal of the Chemical Society (Resumed)
External Links
Snippet
Hydrogen peroxide, without a catalyst, converts erucic acid into 13: 14-dihydroxybehenic acid, mp 101", and brassidic acid into the isomer, mp 132", but if osmium tetroxide is present erucic acid gives the derivative of mp 132" and brassidic acid that of mp 101". The allocation …
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 CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O 0 title abstract description 149
Classifications
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- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
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- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
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