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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701364Generated: October 26, 2026

Acetyl chloride → 4-Carbomethoxy-2-methylbutanoic acid

https://huagongshe.com/reaction/1701364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-Methylglutaric AcidHCID 12046—
Reactant4-Methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine saltHCID 70583400—
SolventEthyl AcetateHCID 8857—
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 is evaporated twice from toluene. The residue is dissolved in methanol (4.7 ml.) and 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 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 distribution between ethyl acetate and aqueous acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04192881
Source datasetuspto-grants-1980_03
ORD IDord-f42b1ac147e1438aa0f5d6d0b1b0ae69
Source noteuspto-grants-1980_03