HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 59094095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22994579 | HCID 22994579 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59094095 | HCID 59094095 | 85.5% |
Reaction Steps
A solution of KOH 50% (3 ml) is added to an equimolar solution of 7-(2-methylallyloxy) 8acetyl-3methylflavone (2.61 g, 0.0075 mol) and benzaldehyde (0.8 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 2.8 g of product m.p. 145-47° C., 1H-NMR (CDCl3)δ:1.78 (s, 3H); 2.20 (s, 3H); 4.62 (s, 2H); 4.98 (d, 2H, J=18 Hz); 7.06 (d,1H, J=16 Hz); 7.09 (d, 1H, J=8.9 Hz); 7.35-7.45 (m,7H); 7.50-7.55(m, 4H); 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-a3e96190dc1d4bbbacf9af092f184b33 |
| Source note | uspto-grants-2003_09 |