HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(Methylamino)carbonyl]-2-(3,3,3-trifluoropropyl)benzenesulfonamide → HCID 10684051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(Methylamino)carbonyl]-2-(3,3,3-trifluoropropyl)benzenesulfonamide | HCID 15270894 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 10684051 | HCID 10684051 | — |
Reaction Steps
40.3 g of N-[2-(3,3,3-trifluoropropyl)-phenylsulfonyl]-N'-methylurea are suspended in 700 ml of chlorobenzene, and dried by the azeotropic distilling off of about 150 ml of solvent. There are then introduced at 120°-130° C. 71 g of phosgene in the course of 90 minutes. The yield after complete concentration of the formed solution by evaporation is 37.3 g of 2-(3,3,3-trifluoropropyl)-phenylsulfonylisocyanate in the form of yellowish oil, which can be directly further reacted.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04759793 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-43e251473bd244dea25461d8a576e3a5 |
| Source note | uspto-grants-1988_07 |