HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1818902Erstellt: 25. Oktober 2026
Tetrahydrofuran → 2,4-Dimethyl-6-phenyl-nicotinonitrile
https://huagongshe.com/reaction/1818902
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | Magnesium Bromide | HCID 82241 | — |
| Edukt | 2-Chloro-4-methyl-6-phenylnicotinonitrile | HCID 833688 | — |
| Katalysator | Copper bromide (CuBr2) | HCID 24611 | — |
| Produkt | 2,4-Dimethyl-6-phenyl-nicotinonitrile | HCID 14090292 | 55% |
Reaktionsschritte
Copper bromide (2.56 g, 17.49 mmol) was suspended in 20 mL of anhydrous THF, dropwisely added with magnesium bromide (3.0M ether, 11.66 mL, 34.99 mmol) at −78° C. and stirred for about 20 minutes. A 10 mL of anhydrous TNF was dropwisely added with a solution, wherein 2 chloro-6-phenyl-4-methyl-nicotinonitrile was dissolved, at the above temperature and then stirred for about 1 hour at room temperature. The mixture was added with a saturated solution of ammonium hydroxide and adjusted its pH to 10 with 1 N NaOH. Then, it was extracted with ethyl acetate, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. A silica gel column chromatography (5% EtOAc/Hexane) was performed on the resulting residue and 550 mg (55%) of 2,4-dimethyl-6-phenyl-nicotinonitrile was obtained in white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07601736B2 |
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| Quelldatensatz | uspto-grants-2009_10 |
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| ORD ID | ord-5c6b5aac4ccc4e76b5d1180c1520fc4d |
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| Quellennotiz | uspto-grants-2009_10 |
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