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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815809Generated: October 29, 2026

Sodium Hydroxide → 7-bromobenzofuran-5-carboxylic acid

https://huagongshe.com/reaction/1815809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22144801HCID 22144801—
SolventEthanolHCID 702—
Product7-bromobenzofuran-5-carboxylic acidHCID 2214475182%

Reaction Steps

A solution of 0.52 gm (2.03 mMol) 5-methoxycarbonyl-7-bromobenzofuran and 0.41 gm (10.13 mMol) sodium hydroxide in 4 mL ethanol was stirred at room temperature until all of the starting material had been consumed. The reaction mixture was concentrated under reduced pressure and the residue dissolved in water. This solution was then made basic by the addition of 1N sodium hydroxide and was extracted well with ethyl acetate. The remaining aqueous phase was made acidic (pH about 2) by treatment with potassium hydrogen sulfate and the resulting solid removed by filtration. The aqueous phase was extracted well with ethyl acetate and the organics were combined and concentrated under reduced pressure to provide 0.40 gm (82%) of 5-carboxy-7-bromobenzofuran as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881733B1
Source datasetuspto-grants-2005_04
ORD IDord-d3f03d001fa9448e8b36a99372e56e74
Source noteuspto-grants-2005_04