HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfanilamide → 4-sulfamoyl-N-[4-(2-furyl)benzylidene]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | 4-(Furan-2-yl)benzaldehyde | HCID 2772295 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-sulfamoyl-N-[4-(2-furyl)benzylidene]aniline | HCID 22316731 | — |
Reaction Steps
A mixture of 2-(4-formylphenyl)furan (0.335 g, 1.95 mmol, prepared according to the method of Heterocycles, 1990, 31, 1951), sulfanilamide (0.336 g, 1.95 mmol) in ethanol (8 mL) was heated at reflux temperature for 2.5 hour. After cooling to room temperature, the crystals which collected by filtration and washed with ethanol to give the subtitle compound (0.378 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06949536B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-5208b50a82624ff28da19943635fcb99 |
| Source note | uspto-grants-2005_09 |