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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232930Generated: October 25, 2026

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

https://huagongshe.com/reaction/2232930

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 numberUSRE041315E1
Source datasetuspto-grants-2010_05
ORD IDord-25e77246674f4f29b03a7d9940ce5b9e
Source noteuspto-grants-2010_05