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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430768Generated: October 30, 2026

Water → HCID 18351724, compound

https://huagongshe.com/reaction/430768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantPhenacyl bromideHCID 6259—
ReactantPotassium CarbonateHCID 11430—
Reactant7-methoxy-1-benzofuran-3-carboxylic acidHCID 12844603—
ProductHCID 18351724HCID 1835172447%

Reaction Steps

7-methoxy-benzofuran-3-carboxylic acid (294 mg) was dissolved in DMF (5 ml). To this solution, potassium carbonate (237 mg) and phenacyl bromide (342 mg) were added, and the resulting solution was stirred at room temperature for 30 minutes. The reaction mixture was poured into water layer (50 ml) and extracted twice with ethyl acetate (20 ml). The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate. Sodium sulfate was removed by filtration and the solvent was removed under reduced pressure. The residue was dissolved in acetic acid (5 ml) and ammonium acetate (551 mg) was added, followed by refluxing the resulting solution for 4 hours. After cooling the reaction solution to room temperature, the solution was poured into water layer (100 ml) and extracted twice with ethyl acetate (30 ml). The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate. After removing the sodium sulfate by filtration, the solvent was removed under reduced pressure and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=5/1) using silica gel to obtain the desired compound (203 mg, yield: 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323235B1
Source datasetuspto-grants-2001_11
ORD IDord-9f3bc072c7074d9288fb39247d3c3d11
Source noteuspto-grants-2001_11