Reaktion #50449

ord-ce23fcfb611f442d921e046fb423ba08

Reaktionsgleichung

[Li][CH](C)CC
sec-butyllithium
CCN(CC)C(=O)c1ccccc1OC
2-methoxy-N,N-diethyl-benzamide
CN(C)CCN(C)C
tetramethylethylenediamine
CCC=O
propionaldehyde
CCN(CC)C(=O)c1c(OC)cccc1C(C)O
6-(1-hydroxyethyl)-2-methoxy-N,N-diethyl-benzamide

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigedoes not exceed -68° C
  2. 2
    workup.ADDITIONWhen the addition
  3. 3
    Temperaturto warm slowly to room temperature
  4. 4
    workup.STIRRINGis subsequently stirred for one hour
  5. 5
    WaschenThe organic phase is washed with 2N hydrochloric acid
  6. 6
    Trocknenwith saturated sodium chloride solution, dried over anhydrous magnesium sulfate
  7. 7
    Einengenconcentrated by evaporation

Vorschrift

13.7 ml of sec-butyllithium (1.4M in cyclohexane/isopentane) are added dropwise to a solution of 5.2 g of 2-methoxy-N,N-diethyl-benzamide and 2.91 g of tetramethylethylenediamine in 50 ml of absolute tetrahydrofuran in such a manner that the temperature does not exceed -68° C. When the addition is complete, the reaction mixture is stirred at -78° C. for a further hour and then 2.5 ml of propionaldehyde are added. The reaction mixture is allowed to warm slowly to room temperature, is subsequently stirred for one hour and is diluted with 300 ml of diethyl ether. The organic phase is washed with 2N hydrochloric acid and then with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated by evaporation to yield 6-(1-hydroxyethyl)-2-methoxy-N,N-diethyl-benzamide in the form of a crude product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05428002uspto-grants-1995_06