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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465344Generated: November 1, 2026

Triphenylphosphine → (4S)-4-acetylthio-2-pyrrolidone

https://huagongshe.com/reaction/465344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(R)-(+)-4-Hydroxy-2-pyrrolidinoneHCID 185505—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
Product(4S)-4-acetylthio-2-pyrrolidoneHCID 86746170—

Reaction Steps

(4R)-4-Hydroxy-2-pyrrolidone (4.5 g) is suspended in tetrahydrofuran (300 ml), and thereto is added triphenylphosphine (23.4 g). After stirring the mixture for 10 minutes, diethyl azodicarboxylate (14 ml) is added dropwise to the mixture below -10° C., and the mixture is stirred at the same temperature for 10 minutes. Thioacetic acid (6.3 ml) is added dropwise to the reaction mixture below -10° C., and the mixture is stirred at the same temperature for 2 hours, and the solvent is evaporated under reduced pressure. The residue is crystallized from diisopropyl ether, and the precipitate is removed by filtration. The filtrate is concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent, chloroform:ethanol=98:2) to give (4S)-4-acetylthio-2-pyrrolidone (3.8 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153187
Source datasetuspto-grants-1992_10
ORD IDord-8f4df708ec3c4f5cb4e12793f79d9828
Source noteuspto-grants-1992_10