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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228270Generated: October 29, 2026

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

https://huagongshe.com/reaction/2228270

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 (10 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 numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-c1a470b58b794a71805ea1dba978faee
Source noteuspto-grants-2002_07