HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77940Erstellt: 25. Oktober 2026
Acetic Acid → 2-(4-Fluoro-benzyloxy)-5-((E)-2-nitro-vinyl)-pyridine
https://huagongshe.com/reaction/77940
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Nitromethane | HCID 6375 | — |
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Edukt | 6-(4-Fluoro-benzyloxy)-pyridine-3-carbaldehyde | HCID 59255111 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(4-Fluoro-benzyloxy)-5-((E)-2-nitro-vinyl)-pyridine | HCID 59255315 | 98,3% |
Reaktionsschritte
To an acetic acid (20.0 mL) solution of 6-(4-fluoro-benzyloxy)-pyridine-3-carbaldehyde (2.23 g, 9.64 mmol) described in Manufacturing Example 58-1-2 were added nitromethane (2.94 g, 48.2 mmol) and ammonium acetate (1.49 g, 19.3 mmol) under nitrogen atmosphere, which was stirred for 2.5 hours at 105° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. This organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The solvent was evaporated from the filtrate under a reduced pressure to obtain the title compound (2.60 g) as a crude product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841327B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-c64ff263d3a946e18c7b9c7fce7b5220 |
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| Quellennotiz | uspto-grants-2014_09 |
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