HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-(Benzyloxy)-2-[(2,6-dichlorophenyl)imino]-3-methylimidazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178478106 | HCID 178478106 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Benzyloxy)-2-[(2,6-dichlorophenyl)imino]-3-methylimidazolidine | HCID 20513893 | — |
Reaction Steps
16.8 g of 1-(benzyloxy)-2-[(2,6-dichlorophenyl)imino]-imidazolidine are dissolved in 80 ml of dimethylformamide and treated while stirring at room temperature with 1.44 g of sodium hydride. After 1 hour, there is added dropwise thereto a solution of 4 ml of methyl iodide in 20 ml of toluene. The temperature rises to 48°. After 16 hours, the mixture is poured into ice and extracted with ether. The organic phase is washed successively with water, 15 percent tartaric acid solution and water, dried over magnesium sulfate and evaporated in vacuo. The 1-(benzyloxy)-2-[(2,6-dichlorophenyl)imino]-3-methylimidazolidine obtained is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04366160 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-51c6fc9731354f0d837d016876089767 |
| Source note | uspto-grants-1982_12 |