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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404592Generated: October 31, 2026

Water → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine

https://huagongshe.com/reaction/1404592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 418486997%

Reaction Steps

tert-Butyl 4-hydroxypiperidine-1-carboxylate (60.0 g, 0.3 mol, 1.0 eq), methanesulfonyl chloride (37.6 g, 0.33 mol, 1.1 eq), and triethylamine (36.2 g, 0.36 mol, 1.2 eq) in 600 ml of dichloromethane (DCM) was stirred at room temperature overnight. Water (300 ml) was added and the layers were separated. The aqueous layer was extracted with DCM once. The combined organics were washed with brine, dried, and evaporated to a yellowish solid, 80.5 g, in 97% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912330B2
Source datasetuspto-grants-2014_12
ORD IDord-64d6af809f9b4e72b7072c8854cb52cf
Source noteuspto-grants-2014_12