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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404015Generated: October 31, 2026

2-Amino-5-bromobenzoic acid → 2-Amino-5-bromobenzenemethanol

https://huagongshe.com/reaction/2404015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromobenzoic acidHCID 79858—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-bromobenzenemethanolHCID 11030874106.9%

Reaction Steps

To a solution of 2-amino-5-bromobenzoic acid (10.0 g, 46.3 mmol) in THF (150 mL) was added BH3-THF (1M, 231 mL) at room temperature, and the reaction mixture was stirred overnight. An aliquot of the reaction mixture was analyzed by LCMS and indicated that the reaction had proceeded to completion. The reaction was quenched with water (150 mL) and extracted with EtOAc (3×500 mL). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered, and concentrated to afford the title compound (10 g, crude), which was directly used in the next step without further purification. MS (ES+) C7H8BrNO requires: 201. found: 202, 204 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802697B2
Source datasetuspto-grants-2014_08
ORD IDord-b85eb3560ace4fb1bc61cfb13699606a
Source noteuspto-grants-2014_08