HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-(3-Methylbutyl)-4-nitrosopiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-Nitrosopiperazine | HCID 21845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Methylbutyl)-4-nitrosopiperazine | HCID 23461651 | — |
Reaction Steps
A mixture of 3-methyl-1-bromo-butane (3.94 g.), N-nitroso-piperazine (3 g.), anhydrous potassium carbonate (3.6 g.) and a small crystal of potassium iodide in dimethyl formamide was heated at 100° for 2 hours. Solvent was removed under reduced pressure and the residue dissolved in ether and water. The ether extract was separated, dried and evaporated to give an oil which was adsorbed on silica gel. Elution with ethyl acetate gave N-(3-methylbutyl)-N'-nitroso piperazine, further purified by dissolving in dilute acid, washing the acid extract with ether, basifying the acid extract and re-extracting with ether. The yield of colourless oil was 3 g (62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04267175 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-ac059a02315d4494b662560f18c8a284 |
| Source note | uspto-grants-1981_05 |