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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228671Generated: October 26, 2026

Water → Bis(3-fluorophenyl)methanol

https://huagongshe.com/reaction/2228671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
Reactant3-FluorobenzaldehydeHCID 68009—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductBis(3-fluorophenyl)methanolHCID 275825080.3%

Reaction Steps

To a solution of 1-bromo-3-fluorobenzene (10.0 g, 57.1 mmol) in tetrahydrofuran (100 mL) was added n-BuLi (1.6M, 35.7 mL, 62.8 mmol) at −78° C. and the mixture was stirred at that temperature for 20 minutes. To the mixture was added 3-fluorobenzaldehyde (7.80 g, 62.8 mmol) and the resulting mixture was stirred at room temperature for 30 minutes. To this mixture was added water and the product was extracted with ethyl acetate. The extract was washed with water, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure to provide 10.1 g of bis(3-fluorophenyl]methanol. To a solution of this compound (6.60 g, 3.0 mmol) in diisopropylether (50 mL) was added phosphorus tribromide (5.41 g, 20.0 mmol) with ice-cooling and the mixture was stirred at that temperature for 1 hour. This reaction mixture was diluted with water and extracted with diisopropylether. The organic layer was washed with water and saturated with aqueous sodium hydrogen carbonate solution, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure to provide 5.61 g of the title compound. Yield 53%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417213B2
Source datasetuspto-grants-2002_07
ORD IDord-00fbe1e78ef748ef9b345bb5678f4b80
Source noteuspto-grants-2002_07