Ethylene Oxide → 6-Fluoro-2-pyridinepropanol

HRID 963322

Reaktionsgleichung

Reaktionsgleichung von HRID 963322
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.C1C[O:12][CH2:11][CH2:10]1.[Li+].CC([N-]C(C)C)C.C1OC1>O>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][CH2:10][CH2:11][OH:12])[N:3]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of 2-fluoro-6-methylpyridin (27 mmol) in 65 ml of freshly distilled THF was added via syringe 13.5 ml of 2M LDA, and the resulting mixture was stirred at -78° C. for 20 min. To the above cold solution was added 4 ml of 4M ethylene oxide and the mixture was allowed to warm to room temperature which stirring. The mixture was diluted with water, extracted with ether, and the organic layer was washed with water (2×) and brine, and dried over sodium sulfate. The organic solution was concentrated, and the residue was purified by flash chromatography (chloroform/ethanol, 10:1) to yield 1.3 g (30.9%) of 2-fluoro-6-(3-hydroxypropyl)pyridine, as a yellow oil.

Aufarbeitung

  1. temperatureto warm to room temperature which
  2. stirringstirring
  3. extractionextracted with ether
  4. washthe organic layer was washed with water (2×) and brine
  5. dry with materialdried over sodium sulfate
  6. concentrationThe organic solution was concentrated
  7. customthe residue was purified by flash chromatography (chloroform/ethanol, 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-a40c09c9f82c43a7b1fa57d35d1dc6a0
Quelldatensatz
uspto-grants-1998_06
Patentnummer
US05763461

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