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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443801Generated: October 25, 2026

Benzhydrol → 3-(Diphenylmethoxy)piperidine

https://huagongshe.com/reaction/443801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrolHCID 7037—
Reactant3-HydroxypiperidineHCID 23293—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Product3-(Diphenylmethoxy)piperidineHCID 2762417—

Reaction Steps

The starting material is prepared as follows. The mixture of 8.28 g of diphenylmethanol, 5.05 g of 3-hydroxypiperidine and 9.5 g of p-toluene sulfonic acid monohydrate is heated to 160°-165° while evacuating the evolving water rapidly. After the water emission ceases, the mixture is heated to said temperature for 3 hours. It is allowed to cool to room temperature and is partitioned between 2 N aqueous sodium hydroxide and diethyl ether. The organic solution is separated, washed with water and saturated aqueous sodium chloride, dried and evaporated. The residue is taken up in diethyl ether, the solution extracted with 0.1 N hydrochloric acid, the extract washed with diethyl ether and made basic with saturated aqueous ammonia. It is re-extracted with diethyl ether, the extract dried and evaporated, to yield the 3-diphenylmethoxypiperidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261990
Source datasetuspto-grants-1981_04
ORD IDord-ea554102fce5434bb14c8c0a03984330
Source noteuspto-grants-1981_04