Ethyl Acetate → 2-(Pyridin-3-yl)propan-2-ol

HRID 1186354Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1186354
C[Mg]Br.[C:4]([C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)(=[O:6])[CH3:5].[Cl-].[NH4+].[C:15](OCC)(=O)C>O1CCCC1>[OH:6][C:4]([C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)([CH3:15])[CH3:5]

Komponenten

6

Edukt 4

HCID 8857Ethyl AcetateHCID 95893-AcetylpyridineHCID 25517Ammonium ChlorideHCID 178418573HCID 178418573, Verbindung

Produkt 1

HCID 107254032-(Pyridin-3-yl)propan-2-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To methylmagnesium bromide (a 0.96 mol/L solution in tetrahydrofuran, 6.26 mL, 5.97 mmol), a solution of 3-acetylpyridine (362 mg, 2.99 mmol) in tetrahydrofuran (3.6 mL) was slowly added under a nitrogen atmosphere at 0° C., and the mixture was stirred at the same temperature for 1. Then, a saturated aqueous ammonium chloride solution was added to the reaction mixture, and extraction with ethyl acetate was performed, followed by washing with brine and drying over anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and thereby 3-(1-hydroxy-1-methylethyl)pyridine (Compound DG) (415 mg, yield: quantitative) was obtained.

Aufarbeitung

  1. washby washing with brine
  2. dry with materialdrying over anhydrous sodium sulfate
  3. customThe solvent was evaporated off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9d93b4c14a4a40478e6c813c0675fa68
Quelldatensatz
uspto-grants-2014_03
Patentnummer
US08673908B2

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