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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370095Generated: October 30, 2026

Methanesulfonyl chloride → Tert-butyl 4-(methylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/370095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventPyridineHCID 1049—
ProductTert-butyl 4-(methylsulfonyl)piperazine-1-carboxylateHCID 449600492%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-tert-Butoxycarbonylpiperazine (2.94 g, 16.0 mmol) was dissolved in pyridine (8 mL) under nitrogen and the solution cooled to 0° C. Methanesulfonyl chloride (1.5 mL, 19.3 mmol) was added. After 5 minutes, more pyridine was added (5 mL) and the reaction mixture was allowed to warm to ambient temperature. After 40 minutes, the pyridine was removed in vacuo. The residue was dissolved in ethyl acetate (250 mL), washed with 0.1M citric acid (3×125 mL), dried over magnesium sulfate, concentrated in vacuo, and dried under vacuum to give 3.84 g (92%) of N-tert-butoxycarbonyl-N'-methylsulfonylpiperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140351
Source datasetuspto-grants-2000_10
ORD IDord-6e177def99cf45c6a810763db456d431
Source noteuspto-grants-2000_10