HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 930926Erstellt: 25. Oktober 2026
Iodoethane → 3-Bromo-2-chloro-5-(ethylsulfonyl)pyridine
https://huagongshe.com/reaction/930926
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Sodium Sulfite | HCID 24437 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 5-Bromo-6-chloropyridine-3-sulfonyl chloride | HCID 2793626 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-Bromo-2-chloro-5-(ethylsulfonyl)pyridine | HCID 59326565 | — |
Reaktionsschritte
Sodium sulfite (1.755 g, 13.92 mmol) and sodium bicarbonate (1.231 g, 14.65 mmol) were dissolved in water (37 mL) to give a colorless solution. The mixture was heated at 75° C. 3-Bromo-2-chloropyridine-5-sulfonyl chloride (2.132 g, 7.33 mmol) was added portionwise over 1 hour. The reaction mixture was stirred at 75° C. for 1 hour. The mixture was concentrated and N,N-dimethylformamide (13.88 mL) was added. Sodium bicarbonate (1.231 g, 14.65 mmol) and iodoethane (0.589 mL, 7.33 mmol) were added. The resulting mixture was heated to 75° C. for 2 hours and then cooled to ambient temperature. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash chromatography (silica gel, 0-100% ethyl acetate/heptane) to provide the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09296741B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-84952ea5e3604f048e593a31dd7ee4df |
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| Quellennotiz | uspto-grants-2016_03 |
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