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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016676Generated: October 25, 2026

Water → trans-(-)-4-(4-Fluorophenyl)-3-hydroxymethylpiperidine monohydrate

https://huagongshe.com/reaction/1016676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(3S,4R)-4-(4-Fluorophenyl)-3-piperidinemethanolHCID 9855829—
SolventTolueneHCID 1140—
Producttrans-(-)-4-(4-Fluorophenyl)-3-hydroxymethylpiperidine monohydrateHCID 6903925489.45%

Reaction Steps

A 200-ml four-necked glass flask equipped with a thermometer and a reflux condenser was charged with 63 ml of toluene and 10.54 g (50.37 mmol) of (−)-(3S,4R)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine, and the mixture was warmed and dissolved. 1.13 g (62.71 mmol) of water was added to the above mixture at 50° C. to allow to crystallize. Thereafter, the mixture was kept for one hour at a temperature of from 20° to 30° C., and then the crystals were collected by filtration. The obtained crystals were thoroughly washed with 20 ml of toluene, to give white crystals of (−)-(3S,4R)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine monohydrate. Thereafter, the crystals were dried under a reduced pressure at a temperature of 30° C. or lower, and weighed 10.24 g. The yield was 89.45% based on (−)-(3S,4R)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476227B1
Source datasetuspto-grants-2002_11
ORD IDord-8e4e9f87089c46f1b9f46d2e3df1680d
Source noteuspto-grants-2002_11