HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 4-Bromo-2-methoxy-1-(2-nitrovinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 4-Bromo-2-methoxybenzaldehyde | HCID 11053041 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-2-methoxy-1-(2-nitrovinyl)benzene | HCID 67080345 | — |
Reaction Steps
A suspension of 4-bromo-2-methoxybenzaldehyde (1.55 g; 7.2 mmol), methylamine hydrochloride (0.31 g; 50.4 mmol) and sodium acetate (0.38 g; 4.6 mmol) in 3 mL of nitromethane was stirred at ambient temperature. After stirring for 14.5 hours the mixture was diluted with 20 mL water and 40 mL dichloromethane, and the mixture was transferred to a separatory funnel. After shaking, the organic layer was dried over sodium sulfate and evaporated to give 1.74 g of 4-bromo-2-methoxy-1-(2-nitrovinyl)benzene as a light yellow solid. MS (apci, neg) m/z=257.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716498B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-629b5a74697f4313a14e1bff0259c297 |
| Source note | uspto-grants-2014_05 |