HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327174Erstellt: 24. Oktober 2026
p-Nitrophenyl-2-aminothiazol-5-ylsulphone → 5-[(4-Nitrophenyl)sulfonyl]thiazole
https://huagongshe.com/de/reaction/327174
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Nitrophenyl-2-aminothiazol-5-ylsulphone | HCID 1535 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | Hypophosphoric acid | HCID 24536 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Phosphoric Acid | HCID 1004 | — |
| Produkt | 5-[(4-Nitrophenyl)sulfonyl]thiazole | HCID 10707153 | 35,2% |
Reaktionsschritte
To a cooled (-5° C.), stirred solution of 2-amino-5-[(4-nitrophenyl)sulfonyl]thiazole (5.15 g, 18.1 mmol) in 85% phosphoric acid (200 mL) was added dropwise a solution of sodium nitrite (1.56 g, 22.6 mmol) in distilled water (10 mL) at such a rate to maintain the internal temperature between -5° and 5° C. When the addition was complete the reaction mixture was stirred for 1 hour at 0° C. then treated dropwise with 50% hypophosphoric acid (15 mL). After the addition, the ice bath was removed and reaction mixture stirred at room temperature for 3 hours during which time moderate frothing occurred. The brown solution was diluted with water (total volume=1 L), neutralized with 28% ammonium hydroxide and filtered. Flash chromatography of the resulting brown solid (eluted with 5% v/v ethyl acetate in methylene chloride) yielded the title thiazole (1.72 g, 35%) as a yellow solid; mp 168°-170° C. 1H--NMR (250 MHz, d6 --DMSO): 8.32 (d, 2H, J=12.6 Hz, aromatic), 8.45 (d, 2H, J=12.8 Hz, aromatic), 8.74 (s, 1H, aromatic), 9.578 (s, 1H, aromatic). MS (CI, CH4): 271(M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05272163 |
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| Quelldatensatz | uspto-grants-1993_12 |
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| ORD ID | ord-94ed8af1edb24399b0998ff8dde550fc |
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| Quellennotiz | uspto-grants-1993_12 |
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