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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Furfuryltriphenylphosphonium bromide | HCID 11418806 | — |
| Reactant | 4-[Ethyl(5-hydroxypentyl)amino]benzaldehyde | HCID 20605390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(N-ethyl-N-(4-((E)-2-(furan-2-yl)vinyl)phenyl)amino)pentan-1-ol | HCID 58637507 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250121B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-7932f77bf30249689757960a094c7639 |
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| Source note | uspto-grants-2007_07 |
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