HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-(4-Benzylpiperazinyl)1-phenylcyclohexanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 4-Oxo-1-phenylcyclohexanenitrile | HCID 91282 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Benzylpiperazinyl)1-phenylcyclohexanecarbonitrile | HCID 54091494 | 76% |
Reaction Steps
35.0 g of 4-cyano-4-phenylcyclohexanone (0.176 mol), (prepared as disclosed in J. Amer. Chem. Soc. 74, (1972) 773) were dissolved with 31 g of 1-benzylpiperazine (0.176 mol) and 21 g of acetic acid in 200 ml of ethanol and, at room temperature, a solution of 12.5 g of sodium cyanoborohydride (0.19 mol) was slowly added dropwise. The mixture was stirred overnight, and then water was added and the mixture was extracted with dichloromethane. Drying and removal of the solvent by distillation resulted in a residue of 46.6 g (76%) of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371088 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-f94a41dfadc847309d18fd2a95250074 |
| Source note | uspto-grants-1994_12 |