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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437574Generated: October 25, 2026

Hydrochloric Acid → 1-Benzyl-4-(p-trifluoromethylphenoxy)piperidine hydrochloride

https://huagongshe.com/reaction/437574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 1-fluoro-4-(trifluoromethyl)-HCID 67873—
Reactant1-Benzylpiperidin-4-olHCID 78461—
ReactantHCID 178418361HCID 178418361—
SolventIsopropanolHCID 3776—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-4-(p-trifluoromethylphenoxy)piperidine hydrochlorideHCID 20263017—

Reaction Steps

A solution of 40.0 g of 1-benzyl-4-piperidinol in 75 ml. of dimethylformamide is added slowly to a stirred suspension of 6.7 g of a 50% oil dispersion of sodium hydride in 300 ml. of dimethylformamide at 60°-70° C. After addition is complete, heating is continued until no more hydrogen gas is liberated. A solution of 39.5 g of 1-fluoro-4-trifluoromethylbenzene in 50 ml. of dimethylformamide is added slowly while maintaining the reaction temperature at 60°-70° C. After addition is complete, stirring and heating at 70°-75° C. is continued for 16 hours. The mixture is poured into 1 l. of water and extracted with benzene. The combined benzene extracts are washed with water, dried, and solvent is removed under reduced pressure, leaving an oil. The oil is taken up in isopropanol and treated with ethereal-HCl, giving a white solid of 1-benzyl-4-(p-trifluoromethylphenoxy)piperidine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031221
Source datasetuspto-grants-1977_06
ORD IDord-f26bef372c3e4341bd1766ceb86a3f7a
Source noteuspto-grants-1977_06