HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-amino-3-phenyl-3H-indol-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | N-(2-Benzoylphenyl)-2,2-dichloroacetamide | HCID 614210 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-amino-3-phenyl-3H-indol-3-ol | HCID 21568705 | — |
Reaction Steps
2'-Benzoyl-2,2-dichloroacetanilide (50 g.) was suspended in 91% ethanol (750 ml) and treated with a solution of potassium cyanide (30 g) in water (50 ml). The reaction was stirred at room temperature for 40 hours. The crystalline precipitate was filtered off and the mother liquors diluted with water to provide further crops of 2-amino-3-phenyl-3H-indol-3-ol. Total 37 g. The product could be recrystallized from acetonitrile or aqueous dimethylformamide and had a m.p. of 204°-6°C (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931226 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-d4c057cab65e47fc8caa83a718bf18ae |
| Source note | uspto-grants-1976_01 |