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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167870Generated: November 3, 2026

3-Methoxybenzaldehyde → HCID 59047019, compound

https://huagongshe.com/reaction/1167870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 22994580HCID 22994580—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 59047019HCID 5904701957.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620842B2
Source datasetuspto-grants-2003_09
ORD IDord-cc181abf36134ab1b7d92779b2a3edc4
Source noteuspto-grants-2003_09