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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371387Generated: October 30, 2026

Triphenylphosphine → HCID 56609827, compound

https://huagongshe.com/reaction/2371387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(2S,4R)-4-hydroxy-N,N,1-trimethylpyrrolidine-2-carboxamideHCID 45116063—
ReactantHCID 178418634HCID 178418634—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56609827HCID 56609827—

Reaction Steps

(2S,4R)-1-Methyl-2-dimethylaminocarbonyl-4-hydroxypyrrolidine (970 mg) was dissolved in dry tetrahydrofuran (11.1 ml), and triphenylphosphine (2.66 g) was added thereto. To the resultant mixture, diethyl azodicarboxylate (1.60 ml) was added under nitrogen steam while ice-cooling, and the mixture was stirred for 30 minutes. Thioacetic acid (1.45 ml) was added to the mixture under ice-cooling, and stirring was continued for 40 minutes under ice-cooling, followed by allowing to stand overnight. The reaction mixture was diluted with dichloromethane, washed with aqueous potassium carbonate solution and dried over magnesium sulfate. After removal of the solvent by distillation, the residue was purified by silica gel column chromatography to give (2S,4S)-1-methyl-2-dimethylaminocarbonyl-4-acetylthiopyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05093328
Source datasetuspto-grants-1992_03
ORD IDord-acd768fa2c424d1c8e89b38b2b0efafe
Source noteuspto-grants-1992_03