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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877632Generated: November 1, 2026

2,4-Dimethoxybenzoic acid → 5-Bromo-2,4-dimethoxybenzoic acid

https://huagongshe.com/reaction/1877632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxybenzoic acidHCID 7052—
ReactantBromineHCID 24408—
SolventChloroformHCID 6212—
Product5-Bromo-2,4-dimethoxybenzoic acidHCID 1350509778.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 250 mL round-bottomed flask was added chloroform (60 mL) along with 2,4-dimethoxybenzoic acid (2.0 g, 10.98 mmol). The solution was cooled to 0° C. and bromine (0.566 mL, 10.98 mmol) was added dropwise over 5 minutes. The solution was allowed to warm to room temperature and stirred overnight. The resulting solid was filtered, washed with cold chloroform and dried under vacuum to give 2.49 g (8.6 mmol, 78% yield) of 5-bromo-2,4-dimethoxybenzoic acid as a yellow solid. The LC/MS data was obtained on a Shimadzu analytical LC/Micromass Platform LC (ESI+) at 220 nm using the following set of conditions: Phenomenex Luna 3 μm C18, 2×30 mm column, with a gradient of 0-100% B (B=90% HPLC grade acetonitrile/0.1% trifluoroacetic acid/10% HPLC grade water), (A=90% HPLC grade water/0.1% trifluoroacetic acid/10% HPLC grade acetonitrile), in 2 minutes with a 1 minute hold at a rate of 1.0 mL/minute. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.88 (s, 3H), 3.95 (s, 3H), 6.78 (s, 1H), 7.86 (s, 1H). LCMS Rt=1.453 min., m/z 262.99 (M+H), 93% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309558B2
Source datasetuspto-grants-2012_11
ORD IDord-12902cbf7c894110b676ea45af180e60
Source noteuspto-grants-2012_11