HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787984Generated: October 25, 2026
Piperidine → N-(4-(1-Piperidinylsulfonyl)phenyl)acetamide
https://huagongshe.com/reaction/1787984
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-(1-Piperidinylsulfonyl)phenyl)acetamide | HCID 79780 | 52.14% |
Reaction Steps
Piperidine (0.0114 Mol) is added to a solution of 4-acetamidophenylsulfonyl chloride (1.34 g, 0.0057 mol) in dioxane (5 mL). The mixture is heated for 1 hour at 80° C., then part of the solvent is removed by evaporation at reduced pressure, and water is added until precipitation of the resulting sulfonamide. The product is collected by filtration as a white solid (52.14% yield) and used without further purification. m.p. 137° C.-139° C. 1H NMR (acetone-d6): δ 1.35-1.43 (m, 2H); 1.52-1.63 (m, 4H); 2.17 (s, 3H); 2.89-2.95 (m, 4H); 7.68-7.70 (d, 2H, J=7); 7.90-7.92 (d, 2H, J=7); 9.55 (bs, 1H). In a similar fashion, the following sulfonamides were prepared:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511133B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-ed8c67e3d1204add98ebb0a1091f6a59 |
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| Source note | uspto-grants-2009_03 |
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