Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22314793 | HCID 22314793 | — |
Reaction Steps
1-benzylpiperazine (Aldrich Chemical Co., Inc., supra) (6.12 g) was dissolved in 10 mL deionized water and cooled to 0° C. Concentrated hydrochloric acid (3.6 mL) was added to adjust the pH to 5.After warming to room temperature, 3.6 mL cyclohexanone was added, followed by potassium cyanide (2.4 g) in 6 mL deionized water. The solution slowly became cloudy. After 18 hours, the solid was filtered. The solid was dissolved in chloroform, dried over Na2SO4, filtered and the solvent was removed in vacuo to yield pure 1-benzyl-4-(1-cyanocyclohexyl) piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05407834 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-9871ee3b14cd4ed492d69ee9d01d6813 |
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| Source note | uspto-grants-1995_04 |
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