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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881441Generated: October 31, 2026

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

https://huagongshe.com/reaction/881441

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 numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-a6749dc9100d4c8a9447ce0f627b570f
Source noteuspto-grants-2015_03