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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067466Generated: November 1, 2026

Water → HCID 21193678, compound

https://huagongshe.com/reaction/1067466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 21193670HCID 21193670—
ReactantPyridinium hydrobromideHCID 21226041—
SolventChloroformHCID 6212—
ProductHCID 21193678HCID 21193678—

Reaction Steps

To a solution of ethyl[(3-oxo-2,3-dihydrobenzofuran-7-yl)oxy]acetate (1.00 g, 4.23 mmol) in chloroform (30 mL) was added pyridinium hydrobromide perbromide (1.35 g, 4.23 mmol) at 0° C. and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into water. The organic layer was washed with water, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure to provide 1.20 g of ethyl[(2-bromo-3-oxo-2,3-dihydrobenzofuran-7-yl)oxy]acetate. A mixture of this compound (1.20 g, 3.80 mmol) and 1-phenyl-2-thiourea (580 mg, 3.80 mmol) in acetic acid (20 mL) was refluxed for 3 hours. The solvent was then distilled off under reduced pressure. To that residue was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5) to provide 180 mg of the title compound. Yield 12%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248766B1
Source datasetuspto-grants-2001_06
ORD IDord-c83330db65c44854b51adb72dca33477
Source noteuspto-grants-2001_06