Water → 6-(4-Formyl-2-methylphenoxy)nicotinonitrile

HRID 130783

Reaktionsgleichung

Reaktionsgleichung von HRID 130783
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[CH3:10].Cl[C:12]1[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][N:13]=1.C(=O)([O-])[O-].[K+].[K+].O>CC(N(C)C)=O>[CH:6]([C:5]1[CH:8]=[CH:9][C:2]([O:1][C:12]2[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][N:13]=2)=[C:3]([CH3:10])[CH:4]=1)=[O:7]

Komponenten

6

Edukt 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 1399014-Hydroxy-3-methylbenzaldehydeHCID 51520946-Chloro-3-pyridinecarbonitrile

Produkt 1

HCID 597302456-(4-Formyl-2-methylphenoxy)nicotinonitrileAusbeute 89,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 31374DimethylacetamideLösungsmittel

Versuchsvorschrift

Combine 4-hydroxy-3-methyl-benzaldehyde (0.502 g, 3.69 mmol), 6-chloro-nicotinonitrile (0.510 g, 3.68 mmol), and potassium carbonate (1.28 g, 9.26 mmol) in dimethylacetamide (18 mL) and warm to 100° C. After 1 h, cool to ambient temperature, dilute reaction mixture with water (40 mL), and extract with ethyl acetate (3×50 mL). Wash combined organic extracts with water and brine successively, dry over anhydrous magnesium sulfate, filter, and concentrate. Purify the residue by silica gel chromatography (hexanes→ethyl acetate gradient/1.5 L) to provide 0.784 g (89%) of the title compound as a light brown solid: mass spectrum (electrospray): m/z=239.0 (M+1);

Aufarbeitung

  1. additiondilute
  2. extractionextract with ethyl acetate (3×50 mL)
  3. washWash
  4. dry with materialdry over anhydrous magnesium sulfate
  5. filtrationfilter
  6. concentrationconcentrate
  7. customPurify the residue by silica gel chromatography (hexanes→ethyl acetate gradient/1.5 L)

Quellen und Nachweise

ORD-Eintrag
ord-61fa8ecdafb44ee882ddcb421775cd98
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07381719B2

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