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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297052Generated: October 30, 2026

Sodium ethoxide → 5-(N-ethyl-N-(4-((E)-2-(furan-2-yl)vinyl)phenyl)amino)pentan-1-ol

https://huagongshe.com/reaction/1297052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantFurfuryltriphenylphosphonium bromideHCID 11418806—
Reactant4-[Ethyl(5-hydroxypentyl)amino]benzaldehydeHCID 20605390—
SolventEthanolHCID 702—
Product5-(N-ethyl-N-(4-((E)-2-(furan-2-yl)vinyl)phenyl)amino)pentan-1-olHCID 58637507—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a 200 mL flask, 1A (18.47 g, 43.6 mmol) and N-ethyl-N-(4-formyl phenyl)-5-aminopentyl alcohol 1B (10.27 g, 43.6 mmol) were dissolved in anhydrous ethanol (115 mL) under Ar at RT. In a separate flask, sodium ethoxide (2.97 g, 43.6 mmol) was dissolved in anhydrous ethanol (51 mL). The ethanolic sodium ethoxide solution was added by addition funnel to the solution containing the starting reagents. The reaction mixture was then heated to 85° C. and stirred for 4 hours. The reaction mixture was evaporated and the product was extracted into dichloromethane against water. The crude product was purified on silica gel using 1:1 hexane:ethyl acetate. Product 2 was a red viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250121B2
Source datasetuspto-grants-2007_07
ORD IDord-7932f77bf30249689757960a094c7639
Source noteuspto-grants-2007_07