HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → (E)-2-(Benzyloxy)-1-ethoxy-4-(2-nitrovinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 3-(Benzyloxy)-4-ethoxybenzaldehyde | HCID 818573 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (E)-2-(Benzyloxy)-1-ethoxy-4-(2-nitrovinyl)benzene | HCID 86730317 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
3-(Benzyloxy)-4-ethoxy benzaldehyde described in Production Example 15-2 (14.5 g, 56.4 mmol) was dissolved in acetic acid (45 mL), then ammonium acetate (5.22 g, 67.7 mmol) and nitromethane (7.5 mL, 138 mmol) were added under nitrogen atmosphere at room temperature, and the mixture was heated and stirred at 130° C. for 2.5 hours. The mixture was cooled to room temperature and the precipitate was collected by filteration and washed with ethanol to quantitatively obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933099B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-14da2fb00edb4a4eb7b54a86918448d5 |
| Source note | uspto-grants-2015_01 |