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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051676Generated: November 1, 2026

Triethylamine → 1-(Tert-butoxycarbonyl)-2-oxopiperidin-4-yl methanesulfonate

https://huagongshe.com/reaction/1051676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 4-hydroxy-2-oxopiperidine-1-carboxylateHCID 56965728—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(Tert-butoxycarbonyl)-2-oxopiperidin-4-yl methanesulfonateHCID 11807541265,981.703%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 100-mL round-bottom flask was charged with a solution of tert-butyl 4-hydroxy-2-oxopiperidine-1-carboxylate (1.00 g, 4.65 mmol) in dichloromethane (30 mL). Triethylamine (1.03 mL, 7.42 mmol) and 4-dimethylaminopyridine (0.057 g, 0.47 mmol) were added, and the mixture was cooled to 0° C. Methanesulfonyl chloride (0.47 mL, 6.05 mmol) was added dropwise and the resulting solution stirred for 1 h at room temperature. The reaction mixture was washed with water (2×10 mL) and 0.1 M aqueous HCl solution (2×10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to afford tert-butyl 4-(methylsulfonyloxy)-2-oxopiperidine-1-carboxylate (0. 900 g, 66%) as a brown solid. MS (ESI, pos. ion) m/z 294 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388161B2
Source datasetuspto-grants-2016_07
ORD IDord-1cdb8873720f4fefb0ebe78a5a0e43e0
Source noteuspto-grants-2016_07