HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 17884081, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-3,3-dimethylbutane | HCID 76111 | — |
| Reactant | 1-(4-tert-Butylphenyl)piperazine | HCID 781722 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 17884081 | HCID 17884081 | — |
Reaction Steps
5 g (22.9 millimoles) of N-(4-tert-butylphenyl)-piperazine, 8.3 g (68.7 millimoles) of neohexyl chloride, 3.2 g (22.9 millimoles) of potassium carbonate and 3.8 g (22.9 millimoles) of potassium iodide are stirred for 16 hours at 140° C. The mixture is taken up in dichloromethane and dilute sodium hydroxide solution. The organic phase is washed, dried over sodium sulfate and evaporated down under reduced pressure, and the residue is chromatographed over silica gel using 1:1 methyl tert-butyl ether/hexane to give 1.5 g (22% of theory) of a colourless oil (for IR data, see Table 1a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935426 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-ef05bbb7f2d84e48a14e181557c47583 |
| Source note | uspto-grants-1990_06 |