Ethyl Bromide → (Z)-2-(Ethoxymethylene)-4,4-dimethylpentanal

HRID 1921928Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1921928
[CH3:1][C:2]([CH3:8])([CH3:7])[CH2:3][CH2:4][CH:5]=[O:6].C[O-].[Na+].C([O:14][CH3:15])=O.Br[CH2:17][CH3:18]>C1COCC1.C1C=CC=CC=1.CN(C=O)C.O.CO>[CH2:17]([O:6]/[CH:5]=[C:4](/[CH2:3][C:2]([CH3:8])([CH3:7])[CH3:1])\[CH:15]=[O:14])[CH3:18]

Komponenten

10

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

4,4-Dimethylpentanal (4.20 g, 36.8 mmol, Step 2) in 36 mL of THF was added over 4 hours by syringe pump to a solution of sodium methoxide, 25 wt. % in methanol (15.1 ml, 66.2 mmol), 15 mL of methanol, and methyl formate (166 ml, 2685 mmol). Following the addition, the reaction was diluted with benzene (50 mL) and DMF (40 mL). The solvents were distilled off at 90° C. leaving the DMF and residual benzene. Bromoethane (11.0 ml, 147 mmol) was added and the solution was heated at 40° C. for 48 hrs and then cooled. The solution was diluted with water, and the reaction was extracted with ether. The combined organic layers were washed with water, brine, and dried over magnesium sulfate, filtered and concentrated toafford the title compound.

Aufarbeitung

  1. additionthe addition
  2. distillationThe solvents were distilled off at 90° C.
  3. customleaving the DMF and residual benzene
  4. temperaturecooled
  5. extractionthe reaction was extracted with ether
  6. washThe combined organic layers were washed with water, brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated toafford the title compound

Quellen und Nachweise

ORD-Eintrag
ord-48ecdc6aa93a4796954773172a2c8933
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08173810B2

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