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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855653Generated: October 27, 2026

Water → 4-Phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1855653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant4-Piperidinecarbonitrile, 4-phenyl-HCID 181138—
SolventDichloromethaneHCID 6344—
Product4-Phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonitrileHCID 9052099.1%

Reaction Steps

17.2 g (89.8 mmol) of 4-methylbenzenesulfonyl chloride dissolved in 150 ml of dichloromethane are added to a solution of 20 g (89.8 mmol) of 4-phenylpiperidine-4-carbonitrile and 28 ml of triethylamine in 200 ml of dichloromethane. The reaction mixture is stirred for 1 hour at room temperature. The reaction is stopped by adding 200 ml of water, and is then extracted with dichloromethane. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then taken up in diethyl ether and filtered off. 30.3 g of 4-phenyl-1-(toluene-4-sulfonyl)piperidin-4-carbonitrile in the form of a white powder are obtained in a yield of 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962846B2
Source datasetuspto-grants-2015_02
ORD IDord-2eaabe980f6749c8a46d93f8783977e9
Source noteuspto-grants-2015_02