6-Cyclohexenyl-pyridine-2-carboxylic acid → 6-Cyclohexyl-pyridine-2-carboxylic acid

HRID 631957

Reaktionsgleichung

Reaktionsgleichung von HRID 631957
[C:1]1([C:7]2[N:12]=[C:11]([C:13]([OH:15])=[O:14])[CH:10]=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1>C(O)C.[Pd]>[CH:1]1([C:7]2[N:12]=[C:11]([C:13]([OH:15])=[O:14])[CH:10]=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Komponenten

4

Edukt 1

HCID 710872336-Cyclohexenyl-pyridine-2-carboxylic acid

Produkt 1

HCID 681621566-Cyclohexyl-pyridine-2-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

To a solution of 6-cyclohexenyl-pyridine-2-carboxylic acid (0.8 g, 3.94 mmol) in ethanol (50 mL) was added 10% palladium on carbon (20%, 0.16 g) under an atmosphere of nitrogen. The suspension was degassed under vacuum and exchanged with hydrogen several times. The mixture was stirred under hydrogen balloon at ambient temperature overnight. The reaction mixture was filtered through a pad of celite, the pad was washed with ethanol and the combined filtrates were concentrated to dryness. The crude title compound (0.62 g, green oil) was used for the next reaction step without further purification; MS (EI): m/e 206.2 [M+H]+

Aufarbeitung

  1. customThe suspension was degassed under vacuum
  2. filtrationThe reaction mixture was filtered through a pad of celite
  3. washthe pad was washed with ethanol
  4. concentrationthe combined filtrates were concentrated to dryness
  5. customThe crude title compound (0.62 g, green oil) was used for the next reaction step without further purification

Quellen und Nachweise

ORD-Eintrag
ord-2bf48c0b49b441d7ad41efd56c64c5ab
Quelldatensatz
uspto-grants-2016_04
Patentnummer
US09321727B2

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