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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78482Generated: October 26, 2026

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

https://huagongshe.com/reaction/78482

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 numberUS08841334B2
Source datasetuspto-grants-2014_09
ORD IDord-4ed160db595c44a3b2615fb6a663a86b
Source noteuspto-grants-2014_09