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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285917Generated: November 3, 2026

Water → 4-Phenyl-4-(4-trifluoromethylphenoxy)piperidine

https://huagongshe.com/reaction/2285917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 1-fluoro-4-(trifluoromethyl)-HCID 67873—
Reactant4-Phenylpiperidin-4-olHCID 96387—
SolventDimethyl SulfoxideHCID 679—
Product4-Phenyl-4-(4-trifluoromethylphenoxy)piperidineHCID 2126825211.7%

Reaction Steps

A mixture of 4-phenyl-4-piperidinol (7.1 g, 40 mM), DMSO (50 ml) and sodium hydride (2 g of a 50% dispersion in oil) was heated at 80° until homogenous, cooled to ambient temperature and treated with 4-fluorobenzotrifluoride (6.6 g, 40 mM) in DMSO (10 ml). After 24 hours the reaction mixture was poured on to cold water (250 ml) and extracted with ether (2×250 ml). The combined organic layers were washed with brine, dried and the solvent removed under reduced pressure. The residue was triturated with cyclohexane, filtered and the mother liquors evaporated and the residue triturated with pentane. Sublimation of the resulting crystals at 0.1 mm Hg (bath temp. 100°) gave the title compound (1.5 g), m.p. 104°-5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04325953
Source datasetuspto-grants-1982_04
ORD IDord-cd1fba3788f64c05976b042466f52790
Source noteuspto-grants-1982_04