Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694662Generated: November 2, 2026

HCID 86618198, compound → 7-(2-Hydroxy-3-phenylpropoxy)-3-(4-methoxyphenyl)chromen-4-one

https://huagongshe.com/reaction/1694662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86618198HCID 86618198—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product7-(2-Hydroxy-3-phenylpropoxy)-3-(4-methoxyphenyl)chromen-4-oneHCID 67279773—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of cuprous iodide (0.14 g, 0.74 mmol) in tetrahydrofuran (2 ml) was added phenylmagnesium bromide in tetrahydrofuran (1M, 2.22 ml, 2.22 mmol) dropwise at −40° C. After 5 minutes 3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)chromen-4-one (0.24 g, 0.74 mmol) in tetrahydrofuran (4 ml) was added slowly, and stirred at −40° C. for 1 hour. The mixture was quenched with saturated ammonium chloride and water, extracted with ethyl acetate, the organic layer washed with brine, dried over sodium sulfate, and the solvent removed under reduced pressure. The residue was purified by preparative thin layer chromatography, eluting with 10% methanol/methylene chloride, followed by ethyl acetate/hexane 2/3, to provide 7-(2-hydroxy-3-phenylpropoxy)-3-(4-methoxyphenyl)chromen-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158810B2
Source datasetuspto-grants-2012_04
ORD IDord-2862fde44e37486ba03fe1aa1edac50a
Source noteuspto-grants-2012_04