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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083712Generated: November 1, 2026

Acetyl chloride → 4-Carbomethoxy-2-methylbutanoic acid

https://huagongshe.com/reaction/2083712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-Methylglutaric AcidHCID 12046—
Reactant4-Methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine saltHCID 70583400—
Product4-Carbomethoxy-2-methylbutanoic acidHCID 13192897—

Reaction Steps

2-Methylglutaric acid (14.6 g.) and acetyl chloride (26 ml.) are heated in the steam bath for one hour. The mixture is concentrated to dryness in vacuo and the residue evaporated twice from toluene. The residue is dissolved in methanol (4.7 ml.), heated on the steam bath for one hour and concentrated to dryness. The residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.). The crystalline salt is filtered, stirred and treated with boiling ethyl acetate (75 ml.). The insoluble material is filtered off, and the filtrate is concentrated to one-third volume and chilled. The crystals are filtered and dried to yield 11.3 g. of 4-methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt, m.p. 97°-99°. The salt is converted to the free acid by treatment with Dowex 50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04086338
Source datasetuspto-grants-1978_04
ORD IDord-d3d63651ac794ef2a67139836c0ea172
Source noteuspto-grants-1978_04