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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580937Generated: November 2, 2026

3,4,5-Trimethoxybenzaldehyde → HCID 56616028, compound

https://huagongshe.com/reaction/1580937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
Reactant2,9-Dimethyl-4H-pyrido(1,2-a)pyrimidin-4-oneHCID 523985—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 56616028HCID 5661602821.5%

Reaction Steps

To a solution of 2.2g of sodium methoxide in 100ml of absolute methanol is added 3.5g of 2,9-dimethyl-4H-pyrido-[1,2-a]pyrimidin-4-one, followed by 4.0g of 3,4,5-trimethoxybenzaldehyde. The mixture is stirred and heated under reflux for 28 hours. A crystalline solid separates and this is colled and filtered. The solid consists of a mixture of colorless and yellow crystals that are separated manually to give 1.52g of a pale yellow solid, melting point 208° - 210°C. The yellow solid is recrystallized from 35ml of methoxyethanol to yield 1.22g of the title compound, melting point 212°-214°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03935197
Source datasetuspto-grants-1976_01
ORD IDord-6a0f44e2b5ce4de6a7967d862f148455
Source noteuspto-grants-1976_01