HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trichloroaniline → HCID 70545492, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trichloroaniline | HCID 12471 | — |
| Reactant | ethyl N-(2-cyano-3-ethoxyacryloyl)carbamate | HCID 230015 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70545492 | HCID 70545492 | — |
Reaction Steps
2,4,6-Trichloroaniline (0.04 mol) is reacted with α-cyano-β-ethoxy-N-ethoxycarbonylacrylamide (0.04 mol) by heating at reflux in ethanol to yield α-cyano-β-(2,4,6-trichloroanilino)-N-ethoxycarbonylacrylamide, which is cyclized by heating at reflux in 1,2-dichlorobenzene to yield crude product which is chromatographed on silica eluting with chloroform/acetone (3/1) to 5-cyano-1-(2,4,6-trichlorophenyl)uracil, pale yellow crystals, m.p. 245°-247°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04297297 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-a9b1121f31b0477cbc3f0780bec371c9 |
| Source note | uspto-grants-1981_10 |