Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281283Generated: November 1, 2026

Ethanol → 4-methyl-5-vinylisobenzofuran-1(3H)-one

https://huagongshe.com/reaction/2281283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-Bromo-4-methylisobenzofuran-1(3H)-oneHCID 59568711—
CatalystHCID 178418807HCID 178418807—
Product4-methyl-5-vinylisobenzofuran-1(3H)-oneHCID 66643922—

Reaction Conditions

Temperature140 °C

Reaction Steps

5-Bromo-4-methyl-2-benzofuran-1(3H)-one (600 mg, 4.5 mmol), potassium vinyl trifluoroborate (510 mg, 2.2 mmmol), PdCl2(dppf)-CH2Cl2 Adduct (180 mg, 0.220 mmmol), and TEA (0.62 mL, 4.5 mmol) were added to 10 mL ethanol in a 20 mL microwave tube. The tube was sealed and degassed, then heated to 140° C. for 20 minutes. Analysis by LC-MS showed product peak. The reaction mixture was diluted with ethyl acetate, washed with brine twice, dried and evaporated to dryness. The crude product was purified by MPLC chromatography (0-80% ETOAC/Hexane solvent system) to yield 5-ethenyl-4-methyl-2-benzofuran-1(3H)-one. 1H-NMR (500 MHz, CDCl3): δ ppm 7.76 (d, J=8 Hz, 1H), 7.03 (dd, J=11, 17 Hz, 1H), 5.84 (d, J=17 Hz, 1H), 5.55 (d, J=11 Hz, 1H), 5.29 (s, 2H), 2.34 (s, 3H). LC-MS: [M+1]=175.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139585B2
Source datasetuspto-grants-2015_09
ORD IDord-b30910808948456985b52f49072e2a62
Source noteuspto-grants-2015_09