Sulfuric Acid → 6-Chloropyridine-3-carbaldehyde

HRID 130900

Reaktionsgleichung

Reaktionsgleichung von HRID 130900
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#N)=[CH:4][N:3]=1.C1(C)C=CC=CC=1.CC(C[AlH]CC(C)C)C.[OH:26]S(O)(=O)=O>CO>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([CH:6]=[O:26])=[CH:8][CH:9]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Combine 6-chloro-nicotino-nitrile (1.00 g, 7.21 mmol) and toluene (24 mL). Cool the resulting solution at 0° C. and add DIBAL-H (1.0 M in toluene, 7.58 mL, 7.58 mmol) dropwise. Stir the resulting red solution at 0° C. for 1 h. Then, add methanol (2 mL) followed by H2SO4 (aq. 2.0 M, 6 mL). Stir for 1 h at rt. Add CHCl3:isopropanol (3/1, 15 mL) and wash with Rochelle's salt solution (20 mL), followed by NaHCO3 (20 mL) and brine. Dry the combined organic layers over magnesium sulfate, filter and concentrate. Purify by flash chromatography (EtOAc/hexanes 10%) to give the title compound (530 mg, 62%).

Aufarbeitung

  1. stirringStir for 1 h at rt
  2. washAdd CHCl3:isopropanol (3/1, 15 mL) and wash with Rochelle's salt solution (20 mL)
  3. dry with materialDry the combined organic layers over magnesium sulfate
  4. filtrationfilter
  5. concentrationconcentrate
  6. customPurify by flash chromatography (EtOAc/hexanes 10%)

Quellen und Nachweise

ORD-Eintrag
ord-11f65d50ccb94616be56241ee9ec4429
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07381719B2

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