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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501924Generated: November 3, 2026

Ethanol → 5-ethenyl-2-benzofuran-1(3H)-one

https://huagongshe.com/reaction/1501924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-BromophthalideHCID 603144—
CatalystHCID 178418807HCID 178418807—
Product5-ethenyl-2-benzofuran-1(3H)-oneHCID 21106313—

Reaction Steps

5-Bromophthalide (50 g, 235 mmol), potassium vinyl trifluoroborate (62.9 g, 469 mmol), and PdCl2(dppf)-CH2Cl2 Adduct (9.58 g, 11.7 mmol) were added to ethanol (500 mL) then TEA (65.4 mL, 469 mmol) was added. The reaction mixture was degassed then heated at reflux for 8 h. The reaction was worked up by diluting with ethyl acetate and washing with brine twice. The organic layer was dried and evaporated to dryness. The crude product was purified by MPLC (silica, 600 g column) with 25% EtOAc/hexane (3 L) then with 30% EtOAc/Hexane (2 L) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-a3c41ffaa7e5456081c22100489a7b58
Source noteuspto-grants-2015_12