HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-(4-Chlorophenyl)-4,5,6,7-tetrahydro-2h-indazol-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-Chlorocyclohexanone | HCID 13203 | — |
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | 2-Oxocyclohexanecarbonitrile | HCID 220297 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(4-Chlorophenyl)-4,5,6,7-tetrahydro-2h-indazol-3-amine | HCID 20312173 | — |
Reaction Steps
A mixture of 3.6 parts of 4-chlorophenylhydrazine and 2.0 parts of triethylamine in 20.0 parts of toluene was stirred at room temperature for fifteen minutes. To the mixture was added 2.5 parts of 2-cyanocyclohexanone, prepared from commercial 2-chlorocyclohexanone and potassium cyanide [von R. E. Meyer, Helv. Chim. Acta., 16, 1291 (1933)], and a few drops of acetic acid. After refluxing for 2 hours, followed by stirring at room temperature overnight, the reaction mixture was evaporated to remove toluene and was treated with water, extracted with diethyl ether, dried over anhydrous magnesium sulfate and concentrated. Recrystallization from ethanol/water gave 2.6 parts of the compound, m.p. 140°-142°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04108628 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-8840b8dc260a4cfaa2724902b9ab9428 |
| Source note | uspto-grants-1978_08 |