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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606678Generated: November 2, 2026

Ethanol → 15-Methyl-8,11,14-eicosatrienoic acid

https://huagongshe.com/reaction/1606678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 54345286HCID 54345286—
SolventWaterHCID 962—
Product15-Methyl-8,11,14-eicosatrienoic acidHCID 53678994—

Reaction Steps

A mixture of 1.3 g. of methyl 15-methyl-8,11,14-eicosatrienoic acid, 12.8 ml of 95% ethanol, 1.1 g. of potassium hydroxide and 1.1 ml. of water under a nitrogen atmosphere was heated under reflux for 2hours, then water and Skellysolve "B" (mixed hexanes) were added. The aqueous and organic layers were separated and the aqueous layer was made acid with 3N hydrochloric acid, then extracted with ether. The ether extract was washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated leaving a residue comprising 15-methyl-8,11,14-eicosatrienoic acid. The residue was distilled in a short path tube at bath temperatures of about 180°C. and a pressure of about 0.007 mm. The distillate was dissolved in 5% ethyl acetate-benzene and chromatographed over 100 g. of acid washed silica gel. Elution with 600 ml. 5%, 500 ml. 10% and 200 ml. 25% ethyl acetate in benzene, then with 100 ml. of ethyl acetate, collecting 50 ml. fractions, and evaporation of the eluate fractions gave a first peak of 183 mg., followed by a 448 mg. peak comprising 15-methyl-8,11,14-eicosatrienoic acid showing one spot on TLC analysis, and having the following NMR absorptions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953499
Source datasetuspto-grants-1976_04
ORD IDord-51944794580642caa9c57cdd80e63183
Source noteuspto-grants-1976_04