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 (3 X) 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 | US04411839 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-d1b32aaa250e4dd1bff5836cad3b6aa9 |
| Source note | uspto-grants-1983_10 |