HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1110636Erstellt: 27. Oktober 2026
Potassium Cyanide → 3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrile
https://huagongshe.com/reaction/1110636
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Cyanide | HCID 9032 | — |
| Edukt | 2,3-Dichloro-5-(trichloromethyl)pyridine | HCID 94647 | — |
| Edukt | 2,3-Dichloro-5-(trifluoromethyl)pyridine | HCID 112234 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrile | HCID 1473374 | — |
Reaktionsschritte
3-Chloro-2-fluoro-5-(trifluoromethyl)pyridine (obtained as a by-product from the fluorine exchange reaction when converting 2,3-dichloro-5-trichloromethyl pyridine to 2,3-dichloro-5-(trifluoromethyl)pyridine) (40.0 g, 0.2 mole) was put into 270 ml of dimethyl sulfoxide and stirred while potassium cyanide (14.4 g, 0.221 mole) was spooned in over a 20-minute period. The mixture was then stirred for another 20 minutes. The temperature was held between 23° and 28° C. throughout the reaction. The mixture was poured into 600 ml of ice water and the product was extracted into hexane. The hexane was removed on a rotary evaporator. The product was treated with activated charcoal and distilled on a Vigreaux-Claisen still at 108°-110° C. at 30 mm Hg to yield 31.45 g of colorless oil with an analysis of, in percent by weight:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | USRE033478 |
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| Quelldatensatz | uspto-grants-1990_12 |
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| ORD ID | ord-83a99c70e02d43f59a316cbf6e75755e |
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| Quellennotiz | uspto-grants-1990_12 |
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