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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100670Generated: October 31, 2026

Boron tribromide → 4-Piperidin-1-yl-3-trifluoromethyl-phenol

https://huagongshe.com/reaction/2100670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(4-Methoxy-2-trifluoromethyl-phenyl)-piperidineHCID 68812212—
SolventDichloromethaneHCID 6344—
Product4-Piperidin-1-yl-3-trifluoromethyl-phenolHCID 68813128—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of crude 1-(4-Methoxy-2-trifluoromethyl-phenyl)-piperidine in dry DCM (3 mL) cooled to −78° C. is added BBr3 (1M in DCM, 3 eq., 1.2 mL). Following this addition, the cooling bath is removed and the reaction is stirred at 25° C. for 12 hours. Upon completion, the reaction is cooled in an ice bath, and water is added dropwise. The quenched reaction is basified to pH=8 by the slow addition of 10% NaHCO3 (aq). The reaction mixture is diluted with DCM and washed with H2O followed by saturated aqueous NaCl. The organic solution is dried over Na2SO4. After concentration, the residue is purified by silica gel chromatography (3:1 hexanes/EtOAc) to give 4-Piperidin-1-yl-3-trifluoromethyl-phenol. [MS: (ES+) 246.1 (M+1)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572811B2
Source datasetuspto-grants-2009_08
ORD IDord-dc7768751a3f45d1aac363a7059fdbf2
Source noteuspto-grants-2009_08