Reaktion #158528

ord-2af5b3cc46b3465ca14651b00e902d99

Reaktionsgleichung

CCOC(=O)C(C)(Br)C(=O)OCC
Diethyl 2-bromo-2-methylmalonate
[F-].[K+]
potassium fluoride
O=[N+]([O-])c1cccc(O)c1
3-nitrophenol
CCOC(=O)C(C)(Oc1cccc([N+](=O)[O-])c1)C(=O)OCC
diethyl 2-methyl-2-(3-nitrophenoxy)malonate
Ausbeute 80.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    Extraktionextracted with ethyl acetate (3×200 mL)
  3. 3
    WaschenThe organic layer was washed with aq. 1N NaOH (2×75 mL)
  4. 4
    Trocknendried over anhydrous Na2SO4
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated in vacuo

Vorschrift

Diethyl 2-bromo-2-methylmalonate (1.0 g, 3.95 mmole) was added to a stirred suspension of potassium fluoride (0.57 g, 9.8 mmole) in dry DMF (5 mL). After stifling for 20 min at room temperature, 3-nitrophenol (0.55 g, 3.95 mmole) was added. The resulting mixture was stirred at 60° C. for 6 h, cooled to room temperature, diluted with water (30 mL) and extracted with ethyl acetate (3×200 mL). The organic layer was washed with aq. 1N NaOH (2×75 mL), dried over anhydrous Na2SO4, filtered and evaporated in vacuo to provide diethyl 2-methyl-2-(3-nitrophenoxy)malonate (0.89 g, 80%). 1H NMR (CDCl3): δ 7.92 (dd, 1H, J=2.3 and 8.2 Hz), 7.82 (t, 1H, J=2.3 Hz), 7.41 (t, 1H, J=8.2 Hz), 7.30 (dd, 1H, J=2.3 and 8.2 Hz), 4.28 (qt, 4H, J=7.0 Hz), 1.81 (s, 3H), 1.26 (t, 6H, J=7.0 Hz).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822685B2uspto-grants-2014_09