Reaktion #54190

ord-486e7c02789e414b9166eabe4ae356b9

Reaktionsgleichung

CCCCN(CCCC)CCCC
tributylamine
C=CC=O
acrolein
C=CC=O
acrolein
CCOC(=O)C(Br)C(=O)OCC
diethyl bromomalonate
CCCCN(CCCC)CCCC
tributylamine
CCO
ethanol
CCOC(=O)C(CCC=O)C(=O)OCC
yellow oil
CCOC(=O)C(CCC=O)C(=O)OCC
γ,γ-dicarbethoxybutyraldehyde

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile cooling in an ice bath
  2. 2
    workup.WAITThe stirring was continued for an additional 1 to 2 hours without additional cooling
  3. 3
    Sonstigethe ethanol and unreacted acrolein were removed on a rotary evaporator
  4. 4
    workup.ADDITIONThe residue was diluted with 500 ml benzene
  5. 5
    Waschenwashed with 3× 100 ml H2O and 2× 100 ml saturated NaCl solution
  6. 6
    Sonstigerotary evaporated

Vorschrift

First, 100 ml acrolein was added to a solution of 180 g diethyl bromomalonate, 14 g tributylamine, and 600 ml ethanol while cooling in an ice bath. After 2-3 hours, an additional 1.5 g tributylamine and 20 ml acrolein was added. The stirring was continued for an additional 1 to 2 hours without additional cooling. The reaction mixture was neutralized with 7 ml glacial acetic acid and the ethanol and unreacted acrolein were removed on a rotary evaporator. The residue was diluted with 500 ml benzene and washed with 3× 100 ml H2O and 2× 100 ml saturated NaCl solution. The benzene solution was dired over CaSO4 and rotary evaporated to yield 207 g of yellow oil which was indicated to be 48% product by glc.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04147702uspto-grants-1979_04