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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234761Generated: October 26, 2026

4-Bromo-3-methylbenzoic acid → (4-Bromo-3-methylphenyl)methanol

https://huagongshe.com/reaction/234761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-methylbenzoic acidHCID 82131—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-3-methylphenyl)methanolHCID 10987288—

Reaction Conditions

Temperature20 °C

Reaction Steps

93 ml of a 1M solution of borane-tetrahydrofuran complex in tetrahydrofuran are added dropwise to a solution of 10 g (46.5 mmol) of 4-bromo-3-methyl-benzoic acid in 100 ml of tetrahydrofuran at 0° C. under argon. After the reaction mixture has been heated to 20° C., it is stirred at this temperature for 16 hours. The excess borane complex is then destroyed by careful addition of water (end of the evolution of hydrogen), the mixture is extracted twice with in each case 250 ml of ethyl acetate and the combined organic phases are washed twice with in each case 100 ml of saturated sodium bicarbonate solution, water and saturated sodium chloride solution, dried over sodium sulphate and concentrated. The compound is reacted further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596006
Source datasetuspto-grants-1997_01
ORD IDord-b9ae21cd79dc49bf8ce25b4dfb2da715
Source noteuspto-grants-1997_01