HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6848Erstellt: 24. Oktober 2026
Methyl iodide → 4-Acetyl-3-methyl-5-(methylthio)thiophene-2-carbonitrile
https://huagongshe.com/de/reaction/6848
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Chloroacetonitrile | HCID 7856 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Acetylacetone | HCID 31261 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Acetyl-3-methyl-5-(methylthio)thiophene-2-carbonitrile | HCID 2820186 | — |
Reaktionsschritte
To a slurry of 2,4-pentanedione (20 mmol) and K2CO3 (3 equivalents, 60 mmol) in DMF (10 mL) was added CS2 (1.2 equivalents, 24 mmol) and the resulting mixture stirred for 10 minutes. The mixture was cooled to 0° C. then chloroacetonitrile (1.0 equivalent, 20 mmol) was added and the reaction stirred 1 hour then warmed to room temperature and stirred for an additional 2 hours. The reaction mixture was again cooled to 0° C. and methyl iodide (1.05 equivalents, 22 mmol) was added slowly. The resulting mixture was warmed to room temperature. After 12 hours, water was added and the resulting suspension was stirred overnight. The desired product was isolated by filtration after washing with water.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07084159B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-fab1cf601eeb4f96bf3c58d1ce626549 |
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| Quellennotiz | uspto-grants-2006_08 |
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