HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → (E)-2-(Benzyloxy)-1-(2-ethoxyethoxy)-4-(2-nitrovinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 86730338 | HCID 86730338 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (E)-2-(Benzyloxy)-1-(2-ethoxyethoxy)-4-(2-nitrovinyl)benzene | HCID 86730339 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
Ammonium acetate (4.16 g, 53.9 mmol) and nitromethane (6.1 mL, 113 mmol) were added to a solution of 3-(benzyloxy)-4-(2-ethoxyethoxy)benzaldehyde described in Production Example 24-2 (13.5 g, 45.0 mmol) in acetic acid (36 mL) under nitrogen atmosphere at room temperature. The liquid mixture was heated and stirred under reflux at 130° C. for 2 hours. The reaction liquid was allowed to stand to cool to room temperature. 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-eced5d020db44afe87b27b41de7fd1a4 |
| Source note | uspto-grants-2015_01 |