HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → Tert-butoxy-2-(2-nitrovinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 2-tert-Butoxybenzaldehyde | HCID 14955526 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butoxy-2-(2-nitrovinyl)benzene | HCID 67080588 | 103.2% |
Reaction Steps
2-tert-Butoxybenzaldehyde (550 mg, 3.09 mmol) was treated with nitromethane (1167 μL, 21.6 mmol) at ambient temperature in a flask. Solid methylamine hydrochloride (133 mg, 1.98 mmol) and sodium acetate (162 mg, 1.98 mmol) were added and the colorless reaction mixture was stirred rapidly at ambient temperature. After 30 minutes, the reaction mixture started to turn yellow. After 16 hours, the reaction was very yellow and precipitate has formed. Water (20 ml) and dichloromethane (40 ml) were added and the layers partitioned. The dichloromethane layer was dried with sodium sulfate, filtered, and concentrated to provide the title compound (705 mg, 3.19 mmol, 103% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716498B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-e5521fc3af7f46b68c949a3e4e7ad976 |
| Source note | uspto-grants-2014_05 |