HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(3,3,3-trifluoro-1propen-1-yl)phenylsulfonyl]-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Benzenesulfonamide, 2-(3,3,3-trifluoro-1-propenyl)- | HCID 53741182 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-(3,3,3-trifluoro-1propen-1-yl)phenylsulfonyl]-N'-methylurea | HCID 53782727 | 96.2% |
Reaction Steps
5.0 g of 2-(3,3,3-trifluoro-1-propen-1-yl)phenysulfonamide and 1.7 g of methyl isocyanate are suspended in 25 ml of methylene chloride and 3.0 g of triethylamine are added dropwise for 10 minutes, whereupon a clear solution forms. The solution is concentrated, the residue is dissolved in a 5% sodium carbonate solution, and insoluble constituents are removed by filtration. The clear solution is acidified with 10% hydrochloric acid, to give 5.9 g of N-[2-(3,3,3-trifluoro-1-propen-1-yl)phenylsulfonyl]-N'-methylurea as a colorless precipitate with a melting point of 190°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041603 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-0d4e845fce564bffbfac5e183a1b719b |
| Source note | uspto-grants-1991_08 |