HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 4-Cyano-4-(piperidin-1-yl)cyclohexyl benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-(Benzoyloxy)cyclohexanone | HCID 242677 | — |
| Reactant | Piperidine, hydrochloride (1:1) | HCID 2723721 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Cyano-4-(piperidin-1-yl)cyclohexyl benzoate | HCID 13306755 | 75% |
Reaction Steps
4-Benzoyloxycyclohexanone (13.5 g, 62 mmoles), piperidine hydrochloride (8.1 g, 67 mmoles) and potassium cyanide (4.25 g, 65 mmoles) were dissolved in 60 ml of 95% ethanol and 60 ml of water. The mixture was stirred at room temperature for 16 hours (overnight). The resulting solid material was collected by filtration. The filtrate was diluted with 100 ml of water and the solution was extracted with ether. Concentration of the ethereal solution gave more solid material. The combined solid material was recrystallized from 90% ethanol to give 14.5 g of white crystalline solid (mp: 165°-171° C.) in 75% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04446065 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-3f2b1cd117874e938a46920dd877daa0 |
| Source note | uspto-grants-1984_05 |