HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-(4-Nitrobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | HCID 22667753 | HCID 22667753 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Nitrobenzyl)piperidine | HCID 783541 | — |
Reaction Steps
4-nitrobenzyl bromide (24:X=Br) (110 mg, 0.5 mmol), potassium carbonate (352 mg, 2.55 mmol) and sodium iodide (76.5 mg, 0.5 mmol) were added to a dimethylformamide (5mil) solution of the piperidine (23) obtained in the process 1, and then stirred under the argon atmosphere at the room temperature for 2 hours. This was further stirred at 70° C. for 1 hour and was extracted with hexan-ethyl acetate (3:1) mixed solvent, and then washed with water and saturated saline solution, dried and vacuum concentrated, thus obtained a 4-nitrobenzylpiperadine compound (25:R=2,2-dimethylcyclopropane) in the form of a yellow crystal (95 mg, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794378B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-82a7babff15d466b9a01ec6352c3850b |
| Source note | uspto-grants-2004_09 |