Reaktion #1784

ord-13eeac45e3ff4344b45ee3f41e200838

Reaktionsgleichung

CCOC(=O)c1cccnc1C(C)C
2-isopropyl-3-carboethoxypyridine
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
CC(C)c1ncccc1CO
2-isopropyl-3-hydroxymethylpyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthen cooled to 0° C.
  2. 2
    Sonstigequenched with EtOAc (100 μL)
  3. 3
    FiltrationThe mixture was filtered
  4. 4
    Sonstigethe solvent was removed under reduced pressure
  5. 5
    workup.ADDITIONToluene was added
  6. 6
    Sonstigethe solvent was removed under reduced pressure

Vorschrift

The 2-isopropyl-3-carboethoxypyridine (400 mg, 2 mmol) in distilled THF (50 mL) under nitrogen was cooled to 0° C. and lithium aluminum hydride (1M in THF) (2.07 mL) was added dropwise. The reaction was stirred for 18 hours at room temperature then cooled to 0° C. and quenched with EtOAc (100 μL), then H2O (100 μL), then 15% NaOH (100 μL), followed by H2O (300 μL). The mixture was filtered and the solvent was removed under reduced pressure. Toluene was added and the solvent was removed under reduced pressure to give the desired 2-isopropyl-3-hydroxymethylpyridine.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726172uspto-grants-1998_03