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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859772Generated: November 1, 2026

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

https://huagongshe.com/reaction/1859772

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 m/e 345 (M+), 346 M++1);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528535B2
Source datasetuspto-grants-2003_03
ORD IDord-2ab31f7451084a14b760ef798eae336c
Source noteuspto-grants-2003_03