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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86618198 | HCID 86618198 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(2-Hydroxy-3-phenylpropoxy)-3-(4-methoxyphenyl)chromen-4-one | HCID 67279773 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158810B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-2862fde44e37486ba03fe1aa1edac50a |
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| Source note | uspto-grants-2012_04 |
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