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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037903Generated: November 2, 2026

2-Methoxybenzoic acid → 5-Bromo-2-methoxybenzoic acid

https://huagongshe.com/reaction/1037903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxybenzoic acidHCID 11370—
ReactantN-bromobutanimideHCID 67184—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-methoxybenzoic acidHCID 881739—

Reaction Steps

To a solution of 2-methoxybenzoic acid (6 g, 39.4 mmol) in 80 mL of acetonitrile was added N-bromosuccinimide (7.4 g, 41.4 mmol) in 20 mL of acetonitrile. The reaction mixture was warmed to ambient temperature and the mixture was allowed to stir for 16 hours. Additional N-bromosuccinimide (14.8 g, 82.8 mmol) was added and the reaction mixture stirred for an additional 48 hours. The mixture was quenched with 25 mL of H2O and the layers were separated. The aqueous layer was extracted with three 15 mL of portions of CH2Cl2 and the combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 50% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 248, 250 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546583B2
Source datasetuspto-grants-2013_10
ORD IDord-33cf17b0582845fca427e819429703db
Source noteuspto-grants-2013_10