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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473801Generated: October 30, 2026

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

https://huagongshe.com/reaction/473801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869114.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (4.0 g, 20.0 mmol) and triethylamine (4.0 g, 40 mmol) in dichloromethane (50 mL) was added methanesulfonyl chloride (2.8 g, 24.4 mmol) at 0° C. The solution was stirred at 0° C. for 10 min, then at room temperature for 2 h. The reaction mixture was partitioned between 10% citric acid and ethyl acetate. The organic layer was washed with sodium bicarbonate, and brine, dried over sodium sulfate, filtered and concentrated to give tert-butyl 4-(methylsulfonyloxy)piperidine-1-carboxylate (6.4 g, quantitative yield). MS (EI) for C11H21NO5S: 279 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637499B2
Source datasetuspto-grants-2014_01
ORD IDord-0e111a34dc56457fbb9d99b2ea059dd8
Source noteuspto-grants-2014_01