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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390994Generated: October 31, 2026

Tert-butyl 4-(methylsulfonyl)piperidine-1-carboxylate → tert-Butyl 4-(acetylthio)piperidine-1-carboxylate

https://huagongshe.com/reaction/390994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(methylsulfonyl)piperidine-1-carboxylateHCID 22504298—
ReactantHCID 23700354HCID 23700354—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 2249477364.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-methanesulfonyl-piperidine-carboxylic acid tert-butyl ester (2.82 g), sodium thioacetate (2.31 g) and DMF (40 ml) was stirred at 60° C. After 4 hours the reaction mixture was cooled and partitioned between ethyl acetate and brine. The combined organics were dried (MgSO4) and the solvents removed in vacuo. The resulting crude mixture was purified by flash chromatography to yield 4-acetylsulfanyl-piperidine-1-carboxylic acid tert-butyl ester (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-9d16d40425434ea8a3f4369e6c0e7620
Source noteuspto-grants-2013_02