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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931375Generated: November 1, 2026

Ethyl chloroformate → Ethyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/931375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromobenzo[b]furan-3(2H)-oneHCID 10512748—
SolventAcetoneHCID 180—
ProductEthyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylateHCID 58458886—

Reaction Steps

Potassium carbonate (1.66 g, 12 mmol) is added to a solution of 5-bromo-1-benzofuran-3(2H)-one (2.13 g, 10 mmol) in acetone (25 mL). The stirred mixture is treated dropwise with ethyl chloroformate (1.05 mL, 11 mmol). The mixture is then heated at reflux for 18 h. The solids are filtered off and the filtrate concentrated in vacuo. The residue is partitioned between EtOAc and saturated aqueous NaHCO3. The layers are separated and the organic layer washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography (gradient elution with hexanes-EtOAc) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296750B2
Source datasetuspto-grants-2016_03
ORD IDord-591bf07ed2904349b7415ea6bc6a6304
Source noteuspto-grants-2016_03