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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361620Generated: October 31, 2026

Sodium Hydroxide → 3-Bromo-5-hydroxybenzoic acid

https://huagongshe.com/reaction/1361620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Bromo-5-iodobenzoic acidHCID 5182520—
SolventWaterHCID 962—
Product3-Bromo-5-hydroxybenzoic acidHCID 15735511—

Reaction Conditions

Temperature140 °C

Reaction Steps

The title compound was made according to the method described in Org. Proc. Res. rev. 2002, 6, 591-595. To 5-iodo-3-bromo-benzoic acid (500 mg, 1.53 mmol), NaOH (250 mg, 6.1 mmol), Cu2O (240 mg, 1.68 mmol) was added water (4.0 mL)). The mixture was heated for 1.5 h at 140° C. in a sealed tube. The cooled mixture was diluted with water and extracted with CH2Cl2. The aqueous layer was acidified (pH˜2) with TFA and extracted with EtOAc. The organic layer was dried over Na2SO4, filtered, concentrated and purified by reverse-phase HPLC to yield 3-bromo-5-hydroxy-benzoic acid. 1H NMR (400 MHz, DMSO-d6): 10.30 (s, 1H), 7.46 (m, 1H), 7.31 (m, 1H), 7.17 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880000B2
Source datasetuspto-grants-2011_02
ORD IDord-aa0446ab0c694916abb5a6cbef06d2c2
Source noteuspto-grants-2011_02