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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387048Generated: November 1, 2026

4-Bromo-2-methylbenzoic acid → (4-Bromo-2-methylphenyl)methanol

https://huagongshe.com/reaction/2387048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-2-methylphenyl)methanolHCID 2228008890%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromo-2-methyl-benzoic acid (9.88 g, 45.9 mmol) was dissolved in THF (100 ml), and the solution was cooled to 0° C. To this solution, a solution of 1M BH3.THF (91.89 ml, 91.89 mmol) was added at 0° C., and the solution was vigorously stirred for 3 hours at room temperature. The reaction mixture was diluted with cold water (20 mL), washed with a saturated solution of NaHCO3, then extracted with ether 3 times (300 mL). The combined organic ether was washed with brine (250 mL), dried over MgSO4, and concentrated in Vacuo. The residue was purified via flash column chromatography (25% to 55% EtOAc in Hexane) to give white solid (8.24 g, 90% yield). 1H NMR (400 MHz, CDCl3) δ: 2.32 (2 H, s) 4.64 (1 H, d, J=5.81 Hz) 7.20-7.26 (2 H, m) 7.30-7.36 (1 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268835B2
Source datasetuspto-grants-2012_09
ORD IDord-c75f21b394e142aca07357bb7e1d4ee2
Source noteuspto-grants-2012_09