HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-nitroacetate → (E)-Methyl-2-nitro-3-(2,4,6-trimethoxyphenyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-nitroacetate | HCID 17206 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 2,4,6-Trimethoxybenzaldehyde | HCID 70019 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-Methyl-2-nitro-3-(2,4,6-trimethoxyphenyl)acrylate | HCID 86641484 | — |
Reaction Steps
2,4,6-trimethoxybenzaldehyde (20.75 g, 0.105 mol) was dissolved in dichloromethane (300 mL) and to this solution magnesium sulphate (15 g, 0.124 mol), ammonium acetate (10 g, 0.129 mol) and methyl nitroacetate (12.60 g, 0.105 mol) were added and stirred at room temperature for 2 hours. At the end of two hours, water (300 mL) was added to the reaction mass, the organic layer was separated and the aqueous layer extracted with dichloromethane (2×100 mL). The organic layers were combined and concentrated under reduced pressure to give a solid, which was crystallized from methanol (100 mL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951961B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-12de784fbfca4daea0727a347296f570 |
| Source note | uspto-grants-2011_05 |