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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274176Generated: October 31, 2026

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

https://huagongshe.com/reaction/2274176

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 (1 M, 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 numberUS09126951B2
Source datasetuspto-grants-2015_09
ORD IDord-9651fc98adb342a09dbfb9a3dbc384b4
Source noteuspto-grants-2015_09