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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087077Generated: October 26, 2026

Acetyl chloride → (R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acid

https://huagongshe.com/reaction/1087077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant(R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acidHCID 19817647—
SolventTetrahydrofuranHCID 8028—
Product(R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acidHCID 54389912—

Reaction Steps

4.0 g of (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acid, 80 ml of absolute tetrahydrofuran and 5 ml of acetyl chloride are boiled at reflux for 4 hours while stirring. Thereafter, the mixture is evaporated. The residue is filtered through silica gel (granular size 0.2-0.5 mm). The evaporation residue of the fractions which are eluted with ethyl acetate is stirred in diethyl ether. By filtration there is isolated (R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acid of melting point 95°-96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034402
Source datasetuspto-grants-1991_07
ORD IDord-b67f071b0b5e40f1870e812b6b171641
Source noteuspto-grants-1991_07