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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443802Generated: October 30, 2026

Benzhydrol → 4-(Diphenylmethoxy)piperidinium chloride

https://huagongshe.com/reaction/443802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrolHCID 7037—
Reactant4-Hydroxypiperidinium chlorideHCID 16212499—
SolventEthanolHCID 702—
Product4-(Diphenylmethoxy)piperidinium chlorideHCID 44153518—

Reaction Steps

The starting material is prepared as follows: The mixture 268 of diphenylmethanol, 200 g of 4-hydroxypiperidine hydrochloride and 28.8 g of p-toulenesulfonic acid monohydrate is stirred and heated to 160° while reducing the pressure to 0.2 mm Hg with a vacuum pump for 3 hours. It is cooled to 80°, dissolved in 500 ml of ethanol and the solution cooled to 10°. The resulting suspension is filtered, the residue washed with isopropanol and dried at 60°, to yield the 4-diphenylmethoxy-piperidine hydrochloride. It is suspended in 1,800 ml of water, converted into the free base with 125 ml of aqueous ammonia and extracted with diethyl ether and the extract evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261990
Source datasetuspto-grants-1981_04
ORD IDord-49f1418a8e2f4cd698189517829e5e86
Source noteuspto-grants-1981_04