Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,6-Lutidine | HCID 7937 | — |
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | 2,3,4,5,6-Pentafluorobenzenesulfonyl chloride | HCID 70026 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Aniline | HCID 6115 | — |
| Produkt | 2,6-Lutidine hydrochloride | HCID 519116 | — |
Reaktionsschritte
Aniline 9.3 (44.6 g, 268 mmol) and 2,6-lutidine (32.8 mL, 282 mmol) were dissolved in 800 mL of acetone (the aniline only partly dissolved). An addition funnel was charged with C6F5SO2Cl (41.8 mL, 282 mmol) and the sulfonyl chloride was added over 15 minutes. During the addition, the starting material dissolved and a new precipitate (2,6-lutidine hydrochloride) formed. After 30 minutes, the 2,6-lutidine hydrochloride was removed by filtration and the filtrate concentrated under reduced pressure. The brown oily solid so produced was triturated with CH2Cl2 and the solid collected. A second batch of product was obtained by repeating the concentration, trituration, and filtration. After drying under high vacuum, 95.5 g (90%) of sulfonamide 9.4 was obtained as a pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06583165B2 |
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| Quelldatensatz | uspto-grants-2003_06 |
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| ORD ID | ord-dde246ed10664faf9b7ae3be31c59a55 |
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| Quellennotiz | uspto-grants-2003_06 |
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