Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | HCID 21862775 | HCID 21862775 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54299702 | HCID 54299702 | 71.3% |
Reaction Steps
0.32 g (1.25 mmol) of 3-(4-fluorobenzoyl)-2-phenylpropionaldehyde [prepared as described in step (i) above] and 0.26 g (1.5 mmol) of 4-sulfamoylaniline were dissolved in 20 ml of acetic acid, and the mixture was heated under reflux for 4 hours. The solvent was then removed by distillation under reduced pressure and water was added to the residue, which was then extracted with ethyl acetate. The organic extract was washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was applied to a silica gel chromatography column and eluted with a 3:2 by volume mixture of hexane and ethyl acetate, to give 0.35 g (yield 60%) of the title compound as a slightly yellow powder, melting at 192-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05908858 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-19595d0cb47a4e8eb1fa989dec538bd9 |
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| Source note | uspto-grants-1999_06 |
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