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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881413Generated: October 28, 2026

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

https://huagongshe.com/reaction/881413

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 numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-8d9f99504b8b4a41aa335c86119931aa
Source noteuspto-grants-2015_03