HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229099Generated: October 30, 2026
Water → N-(4-(Aminosulphonyl)phenyl)acrylamide
https://huagongshe.com/reaction/2229099
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-(Aminosulphonyl)phenyl)acrylamide | HCID 75803 | — |
Reaction Steps
In 100 mL of tetrahydrofuran was dissolved 17 g of p-aminobenzenesulfonamide. This solution was cooled to 0° C. on an ice bath. To this solution was dropwise added 5 g of acryloyl chloride. After completion of the addition, the ice bath was removed and the reaction mixture was warmed to room temperature and stirred for 1 hour. Subsequently, the reaction mixture was heated at 60° C. for 1 hour. After completion of the reaction, the reaction mixture was poured into 1 L of distilled water. Thus, N-(p-aminosulfonylphenyl)acrylamide was obtained as precipitated white particles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420082B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-67cffc79fe1441e8b245d94d876f9fdf |
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| Source note | uspto-grants-2002_07 |
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