HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167870Generated: November 3, 2026
3-Methoxybenzaldehyde → HCID 59047019, compound
https://huagongshe.com/reaction/1167870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22994580 | HCID 22994580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59047019 | HCID 59047019 | 57.5% |
Reaction Steps
A solution of KOH 50% (3 ml) is added to an equimolar solution of 3-(3-methylbut -2-enyloxy)4acetylxanthen-9one (2.4 g, 0.0075 mol) and 3-methoxy-benzaldehyde (1.01 g, 0.0075 mol) in ethanol 95%, the addition being 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 with methanol to give 1.9 g of product m.p. 134-36° C., 1H-NMR (CDCl3) δ: 1.69 (s, 3H); 1.72 (s, 3H); 3.84 (s, 3H); 4.71 (d, 2H, J=6.5); 5.38-5.40 (m, 1H); 6.95-6.98 (m, 1H); 7.05-7.15 (m, 2H); 7.08 (d, 1H, J=8.8 Hz); 7.09 (d, 1H, J=16 Hz); 7.23-7.42 (m, 4H); 7.65-7.72 (m, 1H); 8.32-8 (d, 1H. J=8.8 Hz); 8.42(d, 1H. J=8.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620842B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-cc181abf36134ab1b7d92779b2a3edc4 |
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| Source note | uspto-grants-2003_09 |
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