HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → TRANS-3-BENZYLOXY-4-METHOXY-BETA-NITROSTYRENE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 3-Benzyloxy-4-methoxybenzaldehyde | HCID 80671 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | TRANS-3-BENZYLOXY-4-METHOXY-BETA-NITROSTYRENE | HCID 688198 | 81% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
Commercially available 3-benzyloxy-4-methoxybenzaldehyde (30 g, 124 mmol) was dissolved in acetic acid (100 mL), then ammonium acetate (10.8 g, 140 mmol) and nitromethane (16.8 mL, 310 mmol) were added under nitrogen atmosphere at room temperature, and the mixture was heated and stirred at 130° C. for 2 hours and 20 minutes. The mixture was cooled to room temperature, then the precipitate was collected by filteration and washed with ethanol to obtain the title compound (28.5 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933099B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-05fdb24916634a0f91f7dd78d069f8e7 |
| Source note | uspto-grants-2015_01 |