HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → N-(t-butoxycarbonyl)-N'-cyclohexyl-N'-methylethylenediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl N-(2-bromoethyl)carbamate | HCID 4103526 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(t-butoxycarbonyl)-N'-cyclohexyl-N'-methylethylenediamine | HCID 22722898 | 72% |
Reaction Steps
To a solution of N-(t-butoxycarbonyl)-2-bromoethylamine (1.0 g) in anhydrous dimethylformamide (15 ml) are added N-methylcyclohexylamine (0.64 ml), anhydrous potassium carbonate (0.9 g) and sodium iodide (2.0 g), and the mixture is stirred at room temperature for three days. Water is added to the reaction mixture, and the whole is extracted with ether. The organic layer is washed with a 10% aqueous sodium hydrogencarbonate solution, water and saturated brine successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography to give 0.82 g (72%) of N-(t-butoxycarbonyl)-N′-cyclohexyl-N′-methylethylenediamine as oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492370B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-0661d0e8c8da47209f1e8e5289cabb4e |
| Source note | uspto-grants-2002_12 |