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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833373Generated: November 2, 2026

Sodium amide → 4-(4-Chlorophenyl)-1-(p-tolylsulphonyl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1833373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium amideHCID 24533—
ReactantN,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
Reactant4-Chlorobenzyl cyanideHCID 241582—
SolventBenzeneHCID 241—
Product4-(4-Chlorophenyl)-1-(p-tolylsulphonyl)piperidine-4-carbonitrileHCID 3016324—

Reaction Steps

To a solution of 60.3 parts of 4-chlorophenylacetonitrile and 118 parts of N,N-bis(2-chloroethyl)-4-toluenesulfonamide in 720 parts of dried benzene under N2 there is added portionwise with stirring at 10°-13° C 32.6 parts of sodamide. The cooling bath is then removed and the mixture is stirred for 1 hour during which time the temperature rises to 70° C and then falls back to 43° C. Ice cold water is added to the mixture and a fine solid forms. This is separated by filtration and washed successively with water and benzene and dried and then triturated in boiling methanol. The undissolved solid is separated by filtration, washed with water and dried to give 1-(4-toluenesulfonyl)-4-(4-chlorophenyl)-4-piperidinecarbonitrile melting at about 202°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066654
Source datasetuspto-grants-1978_01
ORD IDord-d8e88b2033684f5f8d4e02e4ccd70113
Source noteuspto-grants-1978_01