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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037897Generated: October 26, 2026

N-bromobutanimide → 5-Bromo-2-ethoxybenzoic acid

https://huagongshe.com/reaction/1037897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Ethoxybenzoic acidHCID 67252—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-ethoxybenzoic acidHCID 5209920—

Reaction Steps

To a solution of 2-ethoxybenzoic acid (3.3 g, 20.0 mmol) in 75 mL of acetonitrile at 0° C. was added N-bromosuccinimide (3.7 g, 21 mmol) in 15 mL of acetonitrile. The reaction mixture was warmed to ambient temperature and the mixture was allowed to stir for 48 hours. The mixture was quenched with 20 mL of H2O and the layers were separated. The aqueous layer was extracted with three 15 mL portions of CH2Cl2 and the combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 10% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 262, 264 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546583B2
Source datasetuspto-grants-2013_10
ORD IDord-4b95855ec6f34f2c986a742c262e14df
Source noteuspto-grants-2013_10