HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1,3-trimethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1-dimethylurea | HCID 12942080 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1,3-trimethylurea | HCID 20566560 | — |
Reaction Steps
A mixture of sodium hydride (0.48 g; 0.01 mol as 50% dispersion in oil) and THF (25 ml) is prepared and maintained under a nitrogen atmosphere. Then 3-[3-chloro-4-(phenethyloxy)phenyl]-1,1-dimethylurea (3.19 g; 0.01 mol) is added to the above mixture. Hydrogen is evolved and a thick paste forms. After about 15 minutes methyl iodide (1.4 g; 0.01 mol) is added and the reaction mixture stirred for two hours at room temperature. After two hours reaction time the paste redissolves. Next, most of the THF is removed under vacuum, the residue dissolved in methylene chloride. The methylene chloride solution is washed with water, dried over sodium sulfate and evaporated to afford the title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04289903 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-85a6c12f53584df7ad90440c0bf97ed4 |
| Source note | uspto-grants-1981_09 |