HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 9838308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | HCID 9819969 | HCID 9819969 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9838308 | HCID 9838308 | 66.1% |
Reaction Steps
Imidazole (0.63 g) was added to a suspension of 4′,7-diacetoxy-5-methylisoflavan-4-one (0.50 g, 1.4 mmol) in absolute ethanol (20.0 ml) and the mixture was refluxed for 45 min under argon. The solution was concentrated under reduced pressure and distilled water (10 ml) was added to the residue. The mixture was left overnight in the fridge and the resulting precipitate was filtered, washed with water and dried to yield 4′,7-dihydroxy-5-methylisoflavan-4-one (0.25 g, 66%) as a white powder. 1H NMR (d6-acetone): δ 2.51 (s, 3H, Me), 3.76 (t, 1H, J 5.7 Hz, H3), 4.57 (d, 2H, J 7.1 Hz, H2), 6.26 (d, 1H, J 2.2 Hz, H8), 6.35 (d, 1H, J 2.2 Hz, H5), 6.78 (d, 2H, J 8.7 Hz, ArH), 7.11 (d, 2H, J 8.7 Hz, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07488494B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-9bc83026f6b844488bfd7f7d4f682329 |
| Source note | uspto-grants-2009_02 |