(3,5,6-Trifluoro-2-pyridyl)hydrazine → 3,5,6-Trifluoropyridin-2-amine
Reaktionsgleichung
[F:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([F:9])=[C:4]([NH:10]N)[N:3]=1>[Ni].CO>[NH2:10][C:4]1[C:5]([F:9])=[CH:6][C:7]([F:8])=[C:2]([F:1])[N:3]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Charged in a hydrogenation reactor were 100 ml of methanol, 16.3 g of the compound obtained in Step 2 of Example 1 and 8.0 g of Raney nickel catalyst, and H2 gas was introduced therein, followed by allowing the reduction to proceed at room temperature for 12 hours. The reaction mixture was filtered through Cellite® to remove the catalyst. The filtrate was concentrated under a reduced pressure to obtain 13.7 g of the title compound as a solid (purity: 99.1%).
Aufarbeitung
- additionCharged in a hydrogenation reactor
- additionwas introduced
- filtrationThe reaction mixture was filtered through Cellite®
- customto remove the catalyst
- concentrationThe filtrate was concentrated under a reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-939a8de3878a407690cd0c8bdb41caaf
- Quelldatensatz
- uspto-grants-2007_05
- Patentnummer
- US07220863B2
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