HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77898Erstellt: 24. Oktober 2026
Acetic Acid → 4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine
https://huagongshe.com/de/reaction/77898
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Nitromethane | HCID 6375 | — |
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Edukt | 4-(4-Methyl-pyridin-2-yloxymethyl)-benzaldehyde | HCID 59255467 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine | HCID 59255134 | 109,4% |
Reaktionsschritte
To an acetic acid (20.0 mL) solution of 4-(4-methyl-pyridin-2-yloxymethyl)-benzaldehyde (2.60 g, 11.5 mmol) described in Manufacturing Example 43-1-2 were added nitromethane (3.50 g, 57.3 mmol) and ammonium acetate (1.76 g, 22.9 mmol) at room temperature under nitrogen atmosphere, which was stirred for 4 hours at 100° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.40 g) as a crude product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08841327B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-cc6dd927238f4dbab11b01f4a7bf78c3 |
|---|
| Quellennotiz | uspto-grants-2014_09 |
|---|