HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(5-Bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroethene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Ethyl 3-ethoxy-2-nitroprop-2-enoate | HCID 54104329 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(5-Bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroethene | HCID 86741430 | 63.2% |
Reaction Steps
A mixture of 2-ethoxy-1-ethoxycarbonyl-1-nitroethene (5.7 g) and 2-amino-5-bromopyridine (5.2 g) in toluene was heated at reflux with slow removal of the ethanol formed during 2 hours. The reaction mixture was cooled and concentrated in vacuo to give a yellow powder which was triturated with hot ethanol, to give 2-(5-bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroethene (6.0 g) in the form of a pale yellow powder, m.p. 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659727 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-c3a8d47b0aba487a8228d03f5c3e5321 |
| Source note | uspto-grants-1987_04 |