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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391022Generated: October 29, 2026

Triethylamine → Tert-butyl 4-(methylsulfonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/391022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(methylsulfonyl)piperidine-1-carboxylateHCID 22504298—

Reaction Steps

To 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (9.2 g) in dichloromethane (170 ml), stirring at 0° C. was added methane sulphonyl chloride (5.33 ml) and triethylamine (0.24 ml). The reaction mixture was slowly warmed to room temperature and stirred overnight. The reaction mixture was partitioned between chloroform and water. The combined organics were washed with brine and dried (MgSO4). The solvent was removed in vacuo to yield 14 g of 4-methanesulfonyl-piperidine-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-2ddac3947ff84b65ba2d691b82bff1e2
Source noteuspto-grants-2013_02