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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66675Generated: October 25, 2026

Water → (4-Bromophenyl)-(1-methyl-4-piperidinyl)methanone

https://huagongshe.com/reaction/66675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzonitrile, 4-bromo-HCID 12162—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-chloro-N-methylpiperidineHCID 79342—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromophenyl)-(1-methyl-4-piperidinyl)methanoneHCID 20530733—

Reaction Steps

To a stirred and cooled (10°-15° C.) Grignard-complex, previously prepared starting from 13.5 parts of 4-chloro-1-methylpiperidine and 2.4 parts of magnesium in 68 parts of tetrahydrofuran, is added dropwise a solution of 10 parts of 4-bromobenzonitrile in 22 parts of tetrahydrofuran. Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is decomposed by pouring onto a mixture of 50 parts of ammonium chloride in 250 parts of water. The product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 10 parts of (4-bromophenyl)-(1-methyl-4-piperidinyl)methanone as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342870
Source datasetuspto-grants-1982_08
ORD IDord-93eec3e9667745f9b5688539be76b279
Source noteuspto-grants-1982_08