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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884881Generated: November 1, 2026

Benzaldehyde → HCID 85055239, compound

https://huagongshe.com/reaction/1884881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 23504933HCID 23504933—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 85055239HCID 8505523947.7%

Reaction Steps

A solution of KOH 50% (3 ml) is added to an equimolar solution of 4-methyl-7-(3-methylbut-2-enyloxy)-8-acetylcoumarin (2.14 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 ethanol to give 1.34 g of product m.p. 114-16° C., 1H-NMR (CDCl3) δ: 1.69 (s, 3H); 1.72 (s, 3H); 2.44 (d, 3H, J=1.22 Hz); 4.65 (d, 2H, J=6.5 Hz); 5.34-5.38 (m, 1H); 6.16 (d, 1H, J=1.2 Hz); 6.95 (d, 1H, J=8.8 Hz); 7.00 (d, 1H, J=18 Hz); 7.10 (d, 1H); 7.30-7.40 (m, 3H); 7.45-7.52 (m, 12H); 7.61 (d, 1H, J=8.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06767916B2
Source datasetuspto-grants-2004_07
ORD IDord-b64bd0b07d294b0182a5131759d48a3f
Source noteuspto-grants-2004_07