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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088636Generated: November 3, 2026

Thioacetic acid → HCID 15086222, compound

https://huagongshe.com/reaction/1088636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetic acidHCID 10484—
ReactantCalcium HydroxideHCID 6093208—
ReactantHCID 15086221HCID 15086221—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 15086222HCID 15086222—

Reaction Steps

To a solution of calcium hydroxide (2.25 g) and (2S,4R)-1-allyloxycarbonyl-2-(imidazol-1-yl)methyl-4-methanesulfonyloxypyrrolidine (10 g) in 4-methyl-2-pentanone (60 ml) was added dropwise thioacetic S-acid (4.38 ml) with stirring below 45° C. The solvent (18 ml) of the mixture was removed under reduced pressure at 40°-45° C. The resulting suspension was heated at 80°-85° C. for 2 hours. After cooling, water (20 ml) and ethyl acetate (20 ml) was added to the reaction mixture The insoluble material was filtered off and washed with ethyl acetate (30 ml). The filtrate and washing were combined. The organic layer was washed with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo to give (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(imidazol-1-yl)methylpyrrolidine (7.94 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963544
Source datasetuspto-grants-1990_10
ORD IDord-ca0aec8554b0467d9661068f40c66b1c
Source noteuspto-grants-1990_10