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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566083Generated: October 25, 2026

4-Toluenesulfonyl chloride → 1-[(4-Methylphenyl)sulfonyl]-4-phenylpiperidine

https://huagongshe.com/reaction/566083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant4-PhenylpiperidineHCID 69873—
SolventAcetonitrileHCID 6342—
Product1-[(4-Methylphenyl)sulfonyl]-4-phenylpiperidineHCID 416846691.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4-phenylpiperidine (5.0 g) in acetonitrile (100 ml) was added triethylamine (8.64 ml) and then was added dropwise at 0° C. a solution of p-toluenesulfonyl chloride (6.50 g) in acetonitrile (30 ml). The mixture was stirred at 0° C. for 2 hours. Under reduced pressure, the solvent was evaporated, and to the residue was water. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the mixture was concentrated, and the resulting crystals were collected by filtration, which were washed with hexane to give colorless crystals of 1-(4-methylphenylsulfonyl)-4-phenylpiperidine (8.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-0ac11c67b5db44359fa3aad6cd4e8e2a
Source noteuspto-grants-2001_01