Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941624Generated: November 3, 2026

Ethyl Acetate → 1-Pyrrolidinecarboxylic acid, 4-(acetylthio)-2-(hydroxymethyl)-, 2-propen-1-yl ester, (2S,4S)-

https://huagongshe.com/reaction/1941624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant(2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanolHCID 18639172—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
Product1-Pyrrolidinecarboxylic acid, 4-(acetylthio)-2-(hydroxymethyl)-, 2-propen-1-yl ester, (2S,4S)-HCID 2284269290%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of (2S,4R)-1-allyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-methanol (19.32 g: 69.17 mmole) and 90% potassium thioacetate (10.73 g: 89.9 mmole) in dimethylformamide (217 ml) is heated with stirring at 65° C. for 5 hours. To the reaction mixture ethyl acetate (200 ml) and ice water (200 ml) are added. The organic layer is taken, successively washed with aqueous 0.05N-sodium hydroxide, 0.1N-hydrochloric acid, water and saturated brine, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by silica gel chromatography to give (2S,4S)-4-acetylthio-1-allyloxycarbonylpyrrolidine-2-methanol (15.34 g). Yield: 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-065e8f19e9644dc88c811c78c47a0f69
Source noteuspto-grants-1997_12