HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 20077842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 22314793 | HCID 22314793 | — |
| Catalyst | 1,2-Dibromoethane | HCID 7839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20077842 | HCID 20077842 | — |
Reaction Steps
To bromobenzene (0.6 g) and magnesium turnings (0.2 g) in 30 ml dry tetrahydrofuran under nitrogen was added a small crystal of iodine and 10 drops of 1,2-dibromoethane. After small bubbles began to form, the reaction was stirred and heated to reflux for 4 hours. After cooling to room temperature, 1-benzyl-4-(1-cyanocyclohexyl)piperazine (1 g) was added. After 23 hours, the reaction was filtered, 20 ml saturated aqueous ammonium chloride was added and the mixture was extracted with diethyl ether. The ether was dried and removed in vacuo. The residue was chromatographed on silica gel eluted with chloroform to yield pure 1-benzyl-4-(1-phenylcyclohexyl)piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05124457 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-7cacdca12b5d43c194d041a46c6675f4 |
| Source note | uspto-grants-1992_06 |