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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368302Generated: October 29, 2026

4-Pyridinecarboxaldehyde → 6-(2-Imidazole-1-yl-ethoxy)-2-pyridin-4-ylmethylene-3,4-dihydro-2H-naphthalen-1-one

https://huagongshe.com/reaction/368302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
Reactant6-(2-Imidazole-1-yl-ethoxy)-3,4-dihydro-2H-naphthalen-1-oneHCID 15486912—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
Product6-(2-Imidazole-1-yl-ethoxy)-2-pyridin-4-ylmethylene-3,4-dihydro-2H-naphthalen-1-oneHCID 5415633921.7%

Reaction Steps

6-(2-Imidazole-1-yl-ethoxy)-3,4-dihydro-2H-naphthalen-1-one (0.50 g, 1.95 mmol) was reacted with 4-pyridinecarboxaldehyde (0.248 g, 2.3 mmol) in 2.5 mL of 4% KOH for 8 hours at room temperature. The reaction was diluted with water, the resulting mixture was filtered, and the filtrate was extracted into EtOAc. The combined extracts were evaporated to dryness, and the resulting yellow solid was purified twice by flash chromatography (silica gel, 120 g, 9% MeOH in DCM) to afford 0.146 g of a yellow oil which crystallized on standing. Recrystallization from minimal iPrOH afforded the title compound as a light yellow powder (0.041 g, 6%), mp 128.5-129° C.; CI-MS mi/e 345 (M+), 346 (M+ +1);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133303
Source datasetuspto-grants-2000_10
ORD IDord-43aa44ca69be463a86d8eb5736337516
Source noteuspto-grants-2000_10