HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 85069798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86586315 | HCID 86586315 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 85069798 | HCID 85069798 | — |
Reaction Steps
A solution of KOH 50% (3 ml) is added to an equimolar solution of 4-methyl-7-methylallyloxy-8-acetylcoumarin (2.04 g, 0.0075 mol) and 3-methoxybenzaldehyde (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 1.6 g of product m.p. 85-87° C., 1H-NMR (CDCl3) δ: 1.74 (s, 3H); 2.43 (s, 3H); 3.85-3.88 (m, 3H); 4.55 (s, 2H); 4.98 (d, 2H, J=15 Hz); 6,16 (s, 1H); 6.93 (d, 1H, J=8.9 Hz; 7.02 (d, 1H, J=16 Hz); 6.95-7.12 (m, 3H); 7.26 (m, 1H); 7.30 (d, 1H,J=16 Hz); −7.61 (d, 1H, J=8.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06767916B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-e6b03d0cdb4f4c4cbdd0bdb8d0899601 |
| Source note | uspto-grants-2004_07 |