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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424362Generated: October 27, 2026

Methanol → (2-Bromo-5-chlorophenyl)methanol

https://huagongshe.com/reaction/424362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromo-5-chlorobenzoic acidHCID 89027—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromo-5-chlorophenyl)methanolHCID 2336313488.8%

Reaction Steps

To a solution of 2-bromo-5-chlorobenzoic acid (5.49 g, 23.3 mmol) in anhydrous THF (70 mL) under nitrogen was added dropwise a BH3 THF solution (1.0 M, 55 mL) at 0° C. and the reaction mixture was stirred overnight at room temperature. Then the mixture was cooled on an ice bath and MeOH (20 mL) was added dropwise to decompose excess BH3. The resulting mixture was stirred until no bubble was released and then 10% NaOH (10 mL) was added. The mixture was concentrated and the residue was mixed with water (200 mL) and extracted with EtOAc. The residue from rotary evaporation was purified by silica gel column chromatography (5:1 hexane/EtOAc) to give 2-bromo-5-chlorobenzyl alcohol as a white solid (4.58 g, 88%): 1H NMR (300 MHz, DMSO-d6): δ (ppm) 7.57 (d, J=8.7 Hz, 1H), 7.50-7.49 (m, 1H), 7.28-7.24 (m, 1H), 5.59 (t, J=6.0 Hz, 1H), 4.46 (d, J=6.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106031B2
Source datasetuspto-grants-2012_01
ORD IDord-29759bc600d64eb9a34f7576918d991c
Source noteuspto-grants-2012_01