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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028980Generated: October 26, 2026

2-Bromo-3-methylbenzoic acid → (2-Bromo-3-methylphenyl)methanol

https://huagongshe.com/reaction/1028980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-methylbenzoic acidHCID 2735588—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromo-3-methylphenyl)methanolHCID 52987706—

Reaction Steps

A solution of 2-bromo-3-methylbenzoic acid (4.0 g, 18.60 mmol) in THF (93 mL) was cooled to 0° C. and LAH (1.41 g, 37.2 mmol) added by portion. After the reaction completed, aq. K/Na tartrate was added and the reaction stirred overnight. The aqueous layer was extracted with EtOAc and the organic layer was then washed with water and brine (3× ea.), dried over Na2SO4 and concentrated in vacuo to give (2-bromo-3-methylphenyl)methanol as a clear oil that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-1bb3791f8ee344d5a1de7af82da45c5f
Source noteuspto-grants-2014_05