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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56454Generated: October 23, 2026

Borohydride → (2-Amino-5-bromo-4-chlorophenyl)methanol

https://huagongshe.com/en/reaction/56454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
Reactant2-Amino-5-bromo-4-chlorobenzoic acidHCID 19612050—
SolventTetrahydrofuranHCID 8028—
Product(2-Amino-5-bromo-4-chlorophenyl)methanolHCID 6708101871%

Reaction Steps

To a solution of 2-amino-5-bromo-4-chlorobenzoic acid (9.0 g, 36.0 mmol) in THF (150 mL) was added borohydride in THF (144 mL, 1 M) at room temperature, and the reaction mixture was stirred overnight. The reaction mixture was quenched with methanol (50 mL), and concentrated to a volume of 50 mL. The residue was diluted with water (100 mL) and extracted with ethyl acetate (150 mL×3). The organic layers were separated, combined, washed with water (100 mL) and brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (crude, 6 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434700B2
Source datasetuspto-grants-2016_09
ORD IDord-077a42d133124a1b9775569963818e3b
Source noteuspto-grants-2016_09