HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-(2-Amino-4-chloroanilino)thiophene-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 12658710 | HCID 12658710 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Amino-4-chloroanilino)thiophene-3-carbonitrile | HCID 20387758 | — |
Reaction Steps
3-(4-Chloro-2-nitroanilino)-thiophene-4-nitrile (17.18 g, 0.06 mol) was hydrogenated in ethanol (300 ml) and ethyl acetate (100 ml) using a palladium/charcoal catalyst (3.5 g, 10%) in a Parr hydrogenator to give 3-(4-Chloro-2-aminoanilino)-thiophene-4-nitrile. After two hours, the reaction was complete, the catalyst was filtered off and the solution was evaporated to dryness under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04172831 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-c789539d9c6444a88416f04bbd400978 |
| Source note | uspto-grants-1979_10 |