Oxygen → HCID 21437765, compound

HRID 1660310Notes

Reaction equation

HRID 1660310 reaction equation
[CH:1]([CH:3]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:4]([O:6][CH3:7])=[O:5])=[O:2].[O:24]=O>>[C:1]([CH:3]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:4]([O:6][CH3:7])=[O:5])([OH:24])=[O:2].[CH:1]([CH:3]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:4]([O:6][CH3:7])=[O:5])=[O:2]

Participants

4

Procedure

Friedrich, in an article entitled "Oxidation of Methyl Formylstearate with Molecular Oxygen" at J. Am. Oil Chemists' Soc. 53, pp. 125-129 (1976) reports the use of air or oxygen to form methyl carboxystearate from methyl formylstearate in an emulsion with a soluble rhodium complex. The reuse of catalyst in hydroformylation reactions is described by Awl in an article entitled "Hydroformylation with Recycled Rhodium Catalyst and One-Step Esterification-Acetalation: A Process for Methyl 9(10)-Methoxymethylenestearate from Oleic Acid," which is printed in J. Am. Oil Chemists' Soc. 53, pp. 190-195 (1976).

Sources & evidence

ORD record
ord-eafea01a1e3947db892644baac8a3481
Source dataset
uspto-grants-1981_12
Patent number
US04307224

Reaction notes

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