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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561418Generated: October 26, 2026

Water → alpha-(4-Fluorophenyl)-4-(trifluoromethyl)benzenemethanol

https://huagongshe.com/reaction/561418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productalpha-(4-Fluorophenyl)-4-(trifluoromethyl)benzenemethanolHCID 579773—

Reaction Steps

1.00 g (5.71 mmol) of 4-bromofluorobenzene were dissolved in 10 ml of tetrahydrofuran at −78° C. Addition of 2.2 ml (6.86 mmol) of a 1.6N solution of n-butyllithium in hexane was followed by stirring for 15 min, and then 1.26 g (6.86 mmol) of trifluoro-p-tolualdehyde dissolved in 10 ml of tetrahydrofuran were added dropwise. The mixture was stirred at −78° C. for 1 h and then at RT for 1 h. The reaction solution was mixed with water and dichloromethane, and the phases were separated. The aqueous phase was extracted with dichloromethane, and the combined organic phases were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and filtered, and the solvents were removed in vacuo. The crude product was purified by preparative HPLC (mobile phase: acetonitrile-water gradient). 1.02 g (66% of theory) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-747f0697c3b5470eb5ef7c40241ce08a
Source noteuspto-grants-2011_11