Diethyl Ether → 9-Heptadecanone

HRID 2193828

Reaktionsgleichung

Reaktionsgleichung von HRID 2193828
[CH2:1]([Mg]Br)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:11]([C:19]#N)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C([O:23]CC)C>>[CH3:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][C:19](=[O:23])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Komponenten

4

Edukt 3

HCID 3283Diethyl Ether2×HCID 16715NonanenitrileHCID 178443577HCID 178443577, Verbindung

Produkt 1

HCID 108879-HeptadecanoneAusbeute 71 %

Versuchsvorschrift

A Grignard solution of n-octylmagnesiumbromide in diethylether (2.0 M, 100 mL, 0.2 mol) was slowly added via syringe to a stirred mixture of n-octylcyanide (13.92 g, 0.1 mol) in diethyl ether (100 mL) at 0° C. under N2 atmosphere. After stirring for 12 h at reflux temperature, the reaction was quenched with an aqueous HCl-solution (2.0 M, 50 mL) at 0° C. and subsequently vigorously stirred for an additional 3 h at room temperature. The organic phase was separated and the aqueous phase was extracted with diethylether. The combined organic phases were washed with a saturated bicarbonate solution and brine, dried over MgSO4 and evaporated under reduced pressure to give an orange solid. The resulting solid was purified recrystallization from methanol to afford yellow crystals (VIII) (18.06 g, 71%). 1H-NMR (CDCl3): δ=2.33 (t, J=7.4 Hz, 4H), 1.58-1.44 (m, 4H), 1.30-1.10 (s, 20H), 0.82 (t, J=6.4 Hz, 6H). 13C-NMR (CDCl3): δ=212.33, 43.42, 32.44, 30.01, 29.90, 29.78, 24.49, 23.26, 14.70.

Aufarbeitung

  1. temperatureat reflux temperature
  2. customthe reaction was quenched with an aqueous HCl-solution (2.0 M, 50 mL) at 0° C.
  3. stirringsubsequently vigorously stirred for an additional 3 h at room temperature
  4. customThe organic phase was separated
  5. extractionthe aqueous phase was extracted with diethylether
  6. washThe combined organic phases were washed with a saturated bicarbonate solution and brine
  7. dry with materialdried over MgSO4
  8. customevaporated under reduced pressure
  9. customto give an orange solid
  10. customThe resulting solid was purified
  11. customrecrystallization from methanol

Quellen und Nachweise

ORD-Eintrag
ord-f744763f35c64fda9311a45d4a2a02e9
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329923B2

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