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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972314Generated: November 3, 2026

Water → Tert-butyl 4-(methylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1972314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(methylsulfonyl)piperazine-1-carboxylateHCID 449600498.6%

Reaction Steps

Methanesulfonyl chloride (34.38 ml, 443 mmol, 1.1 equiv.) was added slowly to a solution of 1-(tert-butoxycarbonyl)piperazine 6 (BOC-piperazine, 75 g, 403 mmol, 1.0 equiv.) and triethylamine (67.4 ml, 483 mmol, 1.2 equiv.) in methylene chloride (750 ml) while maintaining the internal temperature below 20° C. The solution was stirred at ambient temperature for 24 hours. The solution was poured onto a mixture of ice and water (1.5 L). The phases were separated and the aq. phase was extracted with methylene chloride (800 ml×2). The organic phases were combined, dried over MgSO4, filtered and concentrated to give tert-butyl 4-(methylsulfonyl)piperazine-1-carboxylate 7 as an off-white solid (105 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431694B1
Source datasetuspto-grants-2013_04
ORD IDord-d10571a9b5af431bb2a5cddc3552dd77
Source noteuspto-grants-2013_04