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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167875Generated: November 2, 2026

3-Methoxybenzaldehyde → HCID 59094103, compound

https://huagongshe.com/reaction/1167875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 22994583HCID 22994583—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 59094103HCID 5909410370.7%

Reaction Steps

A solution of KOH 50% (3 ml) is added to an equimolar solution of 7-allyloxy-8acetyl -3-methylflavone (2.5 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. 90-92° C., 1H-NMR (CDCl3)δ:2.20 (s, 3H); 3.84 (s, 3H); 4.74 (d, 2H, J=5.1 Hz); 5.1-5.3 (m, 2H); 5.91-6.02 (m, 1H); 6.96-7.18 (m, 4H); 7.31 (d, 1H, J=16 Hz); 7.32-7.35 (m, 1H); 7.36-7.43 (m, 3H); 7.55-7.59 (m, 2H); 8.34 (d, 1H, J=8.9Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620842B2
Source datasetuspto-grants-2003_09
ORD IDord-379865829d1d49f6a9b5f557ef1504af
Source noteuspto-grants-2003_09