HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (4-Benzylpiperazin-1-yl)(cyclohexyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (4-Benzylpiperazin-1-yl)(cyclohexyl)methanone | HCID 562738 | 74% |
Reaction Steps
To a solution of 21.2 g (0.12 mole) of 1-benzylpiperazine in 100 ml of CHCl3 was added dropwise over a period of 30 minutes a solution of 15.0 g (0.10 mole) of cyclohexanecarbonyl chloride in 50 ml of CHCl3. The mixture was allowed to stand at room temperature during 45 minutes and was made basic with 5 g of sodium hydroxide in 50 ml of water. The nonaqueous layer was separated, dried over sodium sulphate and concentrated. The residue was distilled b.p. 150°-56° C. at 0.1-0.2 mmHg to give 21.2 g of 1-cyclohexanecarbonyl-4-benzylpiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04492698 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-2f49ef55eced435db77d406044c58ef4 |
| Source note | uspto-grants-1985_01 |