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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603181Generated: November 1, 2026

4-Toluenesulfonyl chloride → (1-Benzylpiperidin-3-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/603181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant(1-Benzylpiperidin-3-yl)methanolHCID 10398044—
SolventDichloromethaneHCID 6344—
Product(1-Benzylpiperidin-3-yl)methyl 4-methylbenzenesulfonateHCID 5765688980.1%

Reaction Steps

To a solution of (1-benzylpiperidin-3-yl)methanol (820 mg) and triethylamine (0.84 mL) in dichloromethane (10 mL) was added para-toluenesulfonyl chloride (846 mg). The solution was stirred overnight at room temperature. The mixture was partitioned between dichloromethane and water. The layers were separated and the organic layer was dried over sodium sulfate and evaporated. The residue was purified by silica column chromatography, eluting with a gradient of 0 to 50% ethyl acetate in hexane to give the title compound as a colourless oil (1.15 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906645B2
Source datasetuspto-grants-2011_03
ORD IDord-ad10acc96531417f85b45d2bffc02a5d
Source noteuspto-grants-2011_03