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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40274Generated: October 26, 2026

4-Bromo-2-chlorobenzoic acid → (4-Bromo-2-chlorophenyl)methanol

https://huagongshe.com/reaction/40274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-chlorobenzoic acidHCID 108829—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-2-chlorophenyl)methanolHCID 43805739—

Reaction Steps

To a stirring solution of 4-bromo-2-chlorobenzoic acid (11.1 g, 47 mmol) in THF (100 mL) at 0° C. under nitrogen was added borane-methyl sulfide complex (9.4 ml, 94 mmol) via syringe over 10 min. Gas evolution quite evident. Ice bath removed, and once gas evolution subsided reaction gently heated to reflux for 1 h. Reaction slowly quenched with MeOH (50 mL) and 2M HCl (20 mL). Aqueous extracted with 9:1 CHCl3/IPA (150 mL). Organic dried with sat NH4Cl, MgSO4, then concentrated to a colorless oil under reduced pressure. Product crystallized after 1 week sitting neat.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-a5ee826e352540d6b4248f3334706d32
Source noteuspto-grants-2013_09