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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584085Generated: October 26, 2026

1-Benzyl-4-piperidone → 1-Benzyl-4-[4-chloro-3-(trifluoromethyl)phenyl]-4-piperidinol

https://huagongshe.com/reaction/584085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant4-Bromo-2-chloro-alpha,alpha,alpha-trifluorotolueneHCID 67959—
SolventDiethyl EtherHCID 3283—
Product1-Benzyl-4-[4-chloro-3-(trifluoromethyl)phenyl]-4-piperidinolHCID 2234518064%

Reaction Steps

A solution of 5-Bromo-2-chlorobenzotrifluoride (5 g, 19.2 mmol) in dry diethyl ether (40 ml) was added dropwise at room temperature to a mixture of Mg (470 mg) in dry diethyl ether (20 ml) under a stream of Argon (g). The reaction gave rise to a solution of Grignard's reagent. A solution of 1-benzyl-4-piperidone (1.3 g, 6.88 mmol) in dry diethyl ether (30 ml) was added dropwise via syringe at room temperature. The combined mixture was stirred for 1 hour, and finally quenched with saturated ammonium chloride solution (40 ml). The mixture was extracted several times with EtOAc and the combined organic phases were dried (MgSO4), filtered and evaporated to dryness. The oily residue was chromathographed on a silica column using EtOAc:toluene (1:1 (v/v)) as eluent affording the title compound (1.6 g, 64%). MS m/z (relative intensity, 70 eV) 369 (M+, 23), 278 (15), 91 (bp), 65 (16), 56 (21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924374B2
Source datasetuspto-grants-2005_08
ORD IDord-85c95e63d57b40e4bffc894f412b49b8
Source noteuspto-grants-2005_08