Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Acetylbenzenesulphonamide | HCID 74065 | 93% |
Reaction Steps
Ex-35A: To a solution of 4-acetylbenzenesulfonyl chloride in acetone (30 mL) was added ammonia (28% in water, 8.2 mL, 57.3 mmol) dropwise at 0° C. The reaction mixture was allowed to stir at 0° C. for 30 min. The precipitate was filtered and the residue was washed with water and dried in vacuo to afford 4-acetylbenzenesulfonamide as a white solid (3.54 g, 93%), mp 176–177° C. 1H NMR (DMSO-d6) δ 8.10 (d, J=9 Hz, 2H), 8.03 (d, J=9 Hz, 2H), 4.86 (brs, 2H), 2.65 (s, 3H). HRMS Calcd. for C8H9NO3S: 199.0303 (M+); Found: 199.0300.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173129B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-e2ab477d03534a64ad6603d737f144ff |
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| Source note | uspto-grants-2007_02 |
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