HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 2-[(1,2-Dichloroethenyl)oxy]benzene-1-sulfonamide | HCID 53712851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-methylurea | HCID 54175902 | 96% |
Reaction Steps
1.9 g of methyl isocyanate are added to a suspension of 6.7 g of 2-(1,2-dichlorovinyloxy)phenylsulfonamide in 50 ml of methylene chloride. 3.3 g of triethylamine are added dropwise to this mixture at 20° to 25° C. in the course of 10 minutes, a clear solution being formed. Stirring of this solution is continued for a further hour, and the solution is then evaporated to dryness. The residue is dissolved in 5% aqueous sodium carbonate solution and acidified with 10% hydrochloric acid, whereupon the product precipitates as crystals. After filtration and drying, 7.8 g of N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-methylurea are obtained. Melting point: 228°-229° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562210 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-ff766e98301c4422a8c30559b1946278 |
| Source note | uspto-grants-1985_12 |