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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216708Generated: October 28, 2026

Water → (4-Bromo-2-methylphenyl)methanol

https://huagongshe.com/reaction/216708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-2-methylphenyl)methanolHCID 22280088—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-bromo-2-methylbenzoic acid (5 g, 22.8 mmol) is dissolved in dry THF (100 ml) and cooled to 0° C. A 1M solution of BH3.THF in THF (34 mL, 34 mmol) is slowly added. The resulting colorless suspension is then stirred overnight, allowing it to gradually reach room temperature. K2CO3 solid (1.1 g) and H2O (100 ml) are added to the colorless solution and the mixture is stirred for an additional 30 minutes. THF is then evaporated and the residue extracted with EtOAc (30 ml). The organic phase is washed with 1N HCl (3×50 ml), dried over Na2SO4 and evaporated. The residue gives the title compound which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193189B2
Source datasetuspto-grants-2012_06
ORD IDord-2927d44e4cc7498981c270d342fcb46c
Source noteuspto-grants-2012_06