HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2298593Erstellt: 24. Oktober 2026
Sodium Chloride → 5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile
https://huagongshe.com/de/reaction/2298593
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Edukt | Hexamethyldisiloxane | HCID 24764 | — |
| Edukt | HCID 18536867 | HCID 18536867 | — |
| Lösungsmittel | 1,1-Dichloroethane | HCID 6365 | — |
| Produkt | 5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile | HCID 18537264 | 59% |
Reaktionsschritte
A slurry of P2O5 (2.7 g, 19 mmol) and hexamethyldisiloxane (6.7 mL) in dichloroethane (13 mL) was heated to 90° C., while stirring under a N2 atmosphere. After stirring for 2 h, the resulting clear solution was allowed to cool to 40° C. 5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxamide (0.9 g, 2.7 mmol) as prepared in previous step was added to this solution and the mixture was heated at 75° C. for 5 h. This solution was cooled to room temperature and stirred with aqueous NaCl (6 M, 100 mL) for 10 min. As the aqueous solution is added a yellow solid precipitated. After 10 min this solid was separated by filtration, and dried under vacuum to give (0.5 g, 59%) of 5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile as a yellow solid. 1H-NMR (DMSO-d6; 300 MHz) δ2.76 (s, 3H), 7.35-7.40 (m, 1H), 7.45-7.50 (m, 2H), 8.05-8.08 (m, 2H), 8.22 (s, 1H), 8.51 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06492403B1 |
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| Quelldatensatz | uspto-grants-2002_12 |
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| ORD ID | ord-d8807b7ea1ca4631b4300d47a6f2b090 |
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| Quellennotiz | uspto-grants-2002_12 |
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