HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(2-Cyano-acetyl)-3-methyl-1-(2-isocyanobenzyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(2-Isocyanobenzyl)-3-methylurea | HCID 58076127 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Propan-2-ol--water (1/1) | HCID 21889133 | — |
| Product | 3-(2-Cyano-acetyl)-3-methyl-1-(2-isocyanobenzyl)-urea | HCID 58076124 | 68% |
Reaction Steps
Under nitrogen atmosphere, 1-(2-isocyanobenzyl)-3-methylurea (98.4 g) and cyanoacetic acid (80.0 g) was added to N,N-dimethylformamide (836 ml). The mixture was stirred at room temperature and methanesulfonyl chloride (72.8 ml) was added dropwise with stirring at this temperature. The mixture was stirred at room temperature for 4 hrs, cooled with water, and water-isopropanol [2:1 (volume ratio), 1670 ml] was added drop wise. The mixture was stirred under water-cooling for 1 hr, and the precipitated crystals were collected by filtration and dried to give 3-(2-cyano-acetyl)-3-methyl-1-(2-isocyanobenzyl)-urea with 68% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841447B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2d62973b998f4ada92c1a893133f91ed |
| Source note | uspto-grants-2014_09 |