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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043760Generated: October 30, 2026

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

https://huagongshe.com/reaction/2043760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 418486989.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,1-dimethylethyl 4-hydroxy-1-piperidinecarboxylate (4.02 g, 20 mmol) and triethylamine (4.4 mL) in 50 mL of dichloromethane was slowly added methanesulfonylchloride (1.7 mL, 22 mmol) at 0° C. The reaction mixture was stirred for 1 h at 0° C., washed with 1 M aqueous hydrochloric acid, dried over MgSO4 and concentrated in vacuo to give 5 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-e3dc494e0cb74936b82b9f793167ef4e
Source noteuspto-grants-2013_11