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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365311Generated: November 2, 2026

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

https://huagongshe.com/reaction/1365311

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 methanesulfonyl chloride (5.33 ml) and triethylamine (10.24 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 numberUS07888352B2
Source datasetuspto-grants-2011_02
ORD IDord-26fce8c7a27b4e8fae0bb6d355c4942e
Source noteuspto-grants-2011_02