HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2308Erstellt: 23. Oktober 2026
Ethylene Glycol → 4-tert-butyl-N-[6-(2-hydroxyethoxy)pyrimidin-4-yl)benzenesulfonamide
https://huagongshe.com/de/reaction/2308
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamide | HCID 10871078 | — |
| Produkt | 4-tert-butyl-N-[6-(2-hydroxyethoxy)pyrimidin-4-yl)benzenesulfonamide | HCID 11783102 | — |
Reaktionsschritte
To ethylene glycol (20 ml) is added sodium hydride (60% dispersion-type, 1.03 g), and thereto is added 4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamide (1.66 g). The mixture is stirred at 60° C. for 20 hours. After cooling, the mixture is acidified with 10% hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer is washed, dried, and evaporated to remove the solvent. The residue is crystallized from ethyl acetate to give 4-tert-butyl-N-{6-(2-hydroxyethoxy)pyrimidin-4-yl}benzenesulfonamide (1.58 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05728706 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-a389d63ceeae4459863ae17f76d2bba8 |
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| Quellennotiz | uspto-grants-1998_03 |
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