HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2,4,6-Trichlorophenyl)hydrazine → alpha-cyano-beta-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2,4,6-Trichlorophenyl)hydrazine | HCID 79234 | — |
| Reactant | ethyl N-(2-cyano-3-ethoxyacryloyl)carbamate | HCID 230015 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | alpha-cyano-beta-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide | HCID 70512904 | — |
Reaction Steps
Four grams (18.9 mmol) of α-cyano-β-ethoxy-N-ethoxycarbonylacrylamide is dissolved in hot ethanol/toluene. To this is added, portionwise, 4 g of 2,4,6-trichlorophenylhydrazine. The mixture is heated to reflux for three days. Cooling of the mixture and evaporation of the solvent gives the crude product, which is recrystallized from ethanol (3X) to yield α-cyano-β-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide, m.p.=161° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04448961 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-9bb6b37eb2dc4b28a309695713d62952 |
| Source note | uspto-grants-1984_05 |