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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764464Generated: October 30, 2026

1-Benzyl-4-piperidone → HCID 22768472, compound

https://huagongshe.com/reaction/1764464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178478997HCID 178478997—
SolventDiethyl EtherHCID 3283—
ProductHCID 22768472HCID 22768472—

Reaction Steps

To a solution of p-chlorobenzylmagnesium chloride in ethyl ether (prepared from 16 parts of p-chlorobenzyl chloride and 3 parts of magnesium turnings in 100 parts of ethyl ether) is added dropwise a solution of 19 parts of N-benzyl-4-piperidone in 50 parts of ethyl ether, the reaction vessel being cooled in an ice bath during the addition. When the addition is complete, mixture is refluxed for 2 hours, cooled, and the Grignard decomposed with saturated ammonium chloride solution. Evaporation of the ethyl ether gives N-benzyl-4-p-chlorobenzyl-4-hydroxypiperidine. ##STR13##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116963
Source datasetuspto-grants-1978_09
ORD IDord-9df930504cde493c91d300ce6569d42b
Source noteuspto-grants-1978_09