Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278188Generated: October 26, 2026

Water → (4-Bromo-3-fluorophenyl)methanol

https://huagongshe.com/reaction/278188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Bromo-3-fluorobenzoic acidHCID 2773341—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-3-fluorophenyl)methanolHCID 20682297—

Reaction Steps

4-Bromo-3-fluorobenzoic acid (40.8 g, 0.187 mol) was dissolved in THF (250 ml) with magnetic stirring under Ar in an ice-H2O bath. The cloudy solution was treated dropwise with borane-THF complex (1 M) (374 mL, 0.374 mol) over a 1 h period maintaining the internal temperature at <10° C. The reaction mixture was left to warm to ambient temperature overnight, then cooled in an ice H2O bath and treated dropwise with H2O (150 mL). The THF was removed on a rotary evaporator, and the residue partitioned between EtOAc and H2O. The aqueous layer was extracted with EtOAc (3×100 mL), the organic layers combined, washed with brine, and dried (Na2SO4), filtered, and concentrated to give the title compound as an oil which solidified on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358985B1
Source datasetuspto-grants-2002_03
ORD IDord-aff96e71042146e085fcca4e95e143c8
Source noteuspto-grants-2002_03