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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523246Generated: October 30, 2026

Ethanol → 2-Amino-4-bromo-5-methylbenzoic acid

https://huagongshe.com/reaction/523246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-4-bromo-5-methylbenzonitrileHCID 117760932—
Product2-Amino-4-bromo-5-methylbenzoic acidHCID 11776130691%

Reaction Steps

A mixture of 2-amino-4-bromo-5-methylbenzonitrile (2.95 g, 14.0 mmol) in a mixture of EtOH (21 mL) and 2 M aqueous NaOH (34.9 mL, 69.9 mmol) was heated at reflux overnight. After cooling to room temperature, the ethanol was removed under reduced pressure, and the aqueous residue was diluted with water. After adjustment of the pH to about 5 with concentrated aqueous HCl, the mixture was stirred for 30 min and the precipitate was collected by filtration and washed with water. The resulting wet solid was dissolved in EtOAc, washed with brine, dried and concentrated to provide 2-amino-4-bromo-5-methylbenzoic acid as a pale yellow solid (2.92 g, 91% yield). Mass spectrum m/z 212, 214 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334290B2
Source datasetuspto-grants-2016_05
ORD IDord-a7d53b41fa4042f78c3f2b0b62fc3eb6
Source noteuspto-grants-2016_05