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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 4-(methylsulfonyl)piperidine-1-carboxylate | HCID 22504298 | — |
| Reactant | HCID 23700354 | HCID 23700354 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 4-(acetylthio)piperidine-1-carboxylate | HCID 22494773 | 64.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993563B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-8d9f99504b8b4a41aa335c86119931aa |
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| Source note | uspto-grants-2015_03 |
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