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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049870Generated: November 2, 2026

Cyanogen Bromide → HCID 20343966, compound

https://huagongshe.com/reaction/2049870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 20344024HCID 20344024—
SolventChloroformHCID 6212—
ProductHCID 20343966HCID 20343966—

Reaction Steps

A solution of 6.8 g of 4-acetyl-1-methyl-4-(2-phenylthiophenyl)piperidine oxalate, Example 6, in 40 ml of chloroform is added dropwise to a rapidly stirring mixture of 14.7 g of potassium carbonate and 3.7 g of cyanogen bromide in 48.5 ml of chloroform. After total addition, the reaction mixture is successively stirred at reflux for 16 hours, filtered, washed five times with 100 ml portions of water, washed with one 50 ml portion of a saturated sodium chloride solution and dried. The resulting product is purified by chromatography (silica gel column, ether eluant) to provide 4-acetyl-1-cyano-4-(2-phenylthiophenyl)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198419
Source datasetuspto-grants-1980_04
ORD IDord-5d01239edcf14a21952237590e089909
Source noteuspto-grants-1980_04