HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Benzenesulfonamide, 4-(5-oxo-3-phenyl-1-imidazolidinyl)-2-(trifluoromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 21528857 | HCID 21528857 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenesulfonamide, 4-(5-oxo-3-phenyl-1-imidazolidinyl)-2-(trifluoromethyl)- | HCID 3041007 | — |
Reaction Steps
2-Phenylamino-N-(3-trifluoromethyl-4-sulphamoylphenyl)-acetamide (11.2g) was added to ethanol (200 ml) and paraformaldehyde (1.3g) in water (400 ml) added thereto under reflux. The mixture was refluxed 11/2 hr, cooled and worked up as in Example 6(c) to yield 11,8 g, m.p. 235°-238°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03963706 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-228ac984b1224e8ab8a2d968ee43975e |
| Source note | uspto-grants-1976_06 |