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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042726Generated: October 26, 2026

2,3,4-Trimethoxybenzoic acid → 5-Bromo-2,3,4-trimethoxybenzoic acid

https://huagongshe.com/reaction/1042726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trimethoxybenzoic acidHCID 11308—
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
Product5-Bromo-2,3,4-trimethoxybenzoic acidHCID 59427885—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2,3,4-trimethoxybenzoic acid (4.7 g, 22 mmol) and NaOAc (5.5 g, 40 mmol) in 35 ml AcOH was added a solution of bromine (1.5 ml, 29 mmol) in 35 ml AcOH. The reaction became red in color, which quickly faded. The mixture was heated to 80° C. for 1 h, at which point it was cooled to ambient temperature. The material was partitioned between dichloromethane and water. The organic layer was removed and the aqueous layer was extracted once with dichloromethane. The combined organic layers were dried with Na2SO4, filtered, and concentrated to give an oil which solidified on standing. The material was dissolved in diethyl ether and hexanes. Concentration to ½ the volume resulted in precipitation of a white solid. Filtration provided the title compound as a white solid. MS m/z: 293 (M+H+); calc'd for C10H11BrO5: 291.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-86887e954fa04ebb8c437c66b3067012
Source noteuspto-grants-2013_10