Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764465Generated: October 30, 2026

Acetic Anhydride → HCID 22768454, compound

https://huagongshe.com/reaction/1764465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 69868284HCID 69868284—
SolventPyridineHCID 1049—
ProductHCID 22768454HCID 22768454—

Reaction Steps

A mixture of 1.0 part of 1-(3,3,3-triphenylpropyl)-4-hydroxy-4-benzyl piperidine hydrochloride, 10 parts by volume of pyridine and 3.0 parts by volume of acetic anhydride is allowed to stand for 24 hours. Volatile material is removed under reduced pressure and the resulting residue is partitioned between dilute sodium hydroxide and ether. The ether layer is separated, washed with water, dried over sodium sulfate and then treated with an excess of a solution of hydrogen chloride in 2-propanol. The solid which forms is separated by filtration and then washed successively with ether, water, and ether, and then air-dried to give 1-(3,3,3-triphenylpropyl)-4-acetoxy-4-benzylpiperidine hydrochloride and having the following structural formula ##STR19## Replacement of acetic anhydride with 3.0 parts of propionic acid anhydride provides 1-(3,3,3-triphenylpropyl)-4-propionyloxy-4-benzylpiperidine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116963
Source datasetuspto-grants-1978_09
ORD IDord-50394441364e4c76b646ad001014998c
Source noteuspto-grants-1978_09