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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986452Generated: October 30, 2026

3-(Trifluoromethyl)benzaldehyde → HCID 14052070, compound

https://huagongshe.com/reaction/986452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 14099895HCID 14099895—
SolventEthanolHCID 702—
ProductHCID 14052070HCID 1405207072.8%

Reaction Steps

In 5 ml of ethanol were dissolved 500 mg of 2-[(E)-3-[4-(3-pyridylmethyl)phenyl]allyloxy]ethyl acetoacetate, 0.20 g of methyl 3-aminocrotonate and 300 mg of 3-trifluoromethylbenzaldehyde, and the resulting solution was subjected to reaction under reflux for 15 hours. Subsequently, the solvent was removed by distillation under reduced pressure, and the residue thus obtained was purified by a column chromatography [Wako Silica Gel C-200, eluant: chloroform:ethanol (100:1 by volume)] to obtain 660 mg (yield 72.8%) of pale yellow, powdery 3-[2-[(E)-3-[4-(pyridin-3-ylmethyl)phenyl]allyloxy]ethyl] 5-methyl 2,6-dimethyl-4-(3-trifluoromethylphenyl)-1,4-dihydropyridine-3,5-dicarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04713387
Source datasetuspto-grants-1987_12
ORD IDord-d5fb78c5b880467595c5adc68b3c4435
Source noteuspto-grants-1987_12