Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 69979331 | HCID 69979331 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59094099 | HCID 59094099 | — |
Reaction Steps
A solution of KOH 50% (3 ml) is added to an equimolar solution of 7-(2-methylallyloxy) -acetyl-3methylflavone (2.61 g, 0.0075 mol) and 3-methoxy-benzaldehyde (1.01 g, 0.0075 mol) in ethanol 95%; the addition is performed under energetic stirring at room temperature. The reaction is left under stirring for one night and then diluted with water and acidified; the precipitate is separated by filtration and dried under vacuum. The compound is crystallized by methanol to give 2.4 g of product m.p. 131-34° C., 1H-NMR (CDCl3)δ:1.76 (s, 3H); 2.20 (s, 3H); 3.82 (s, 3H) 4.62 (s, 2H); 5.05 (d, 2H, J=18 Hz); 6.95-7.10 (m, 3H); 7.09 (d, 1H, J=9 Hz); 7.10 (d, 1H, J=9 Hz); 7.31 (d, 1H, J=16 Hz); 7.40-07.45 (m, 3H); 7.55-7.58 (m, 2H); 7.31 (s, 2H); 8.32 (d, 1H, J=8.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06620842B2 |
|---|
| Source dataset | uspto-grants-2003_09 |
|---|
| ORD ID | ord-de2a90b343b040cb9a475b92b745e408 |
|---|
| Source note | uspto-grants-2003_09 |
|---|