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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941620Generated: November 3, 2026

Potassium ethanethioate → (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-phthalimidomethylpyrrolidine

https://huagongshe.com/reaction/1941620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
Reactant(2S,4R)-1-allyloxycarbonyl-2-phthalimidomethyl-4-methanesulfonyloxypyrrolidineHCID 57022733—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-phthalimidomethylpyrrolidineHCID 5718419581%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of (2S,4R)-1-allyloxycarbonyl-2-phthalimidomethyl-4-methanesulfonyloxypyrrolidine (12.4 g: 30.46 mmole) and 90% potassium thioacetate (5.22 g: 45.69 mmole) in dimethylformamide (130 ml) is heated with stirring at 60° C. for 4 hours. The reaction mixture is diluted with ethyl acetate (200 ml) and ice water (200 ml). The organic layer is taken, successively washed with water (3 times) and saturated brine, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by silica gel chromatography to give crude (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-phthalimidomethylpyrrolidine (9.33 g). Yield: 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-7a80560b24aa4d0b904ee583076a3de6
Source noteuspto-grants-1997_12