Reaktion #1117850

ord-f1eabd7553d241a58f3f3f205ce4c971

Reaktionsgleichung

CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
CCN(CC)CCCCCCO
6-diethylamino-1-hexanol
O=Cc1ccc(O)cc1
4-hydroxy-benzaldehyde
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCN(CC)CCCCCCOc1ccc(C=O)cc1
4- [[6-(diethylamino)hexyl]oxy]benzaldehyde
Ausbeute 64.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the dropwise addition the mixture
  2. 2
    SonstigeThe reaction mixture was then evaporated in a rotary evaporator
  3. 3
    SonstigeThe residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate 7:3)

Vorschrift

A mixture of 2.17 g of 6-diethylamino-1-hexanol (J. Chem. Soc. 1942, 428), 1.52 g of 4-hydroxy-benzaldehyde and 3.3 g of triphenylphosphine in 100 ml of tetrahydrofuran was treated slowly at 20° with a solution of 1.97 g of diethyl azodicarboxylate. After the dropwise addition the mixture was stirred at room temperature for a further 5 hours. The reaction mixture was then evaporated in a rotary evaporator. The residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate 7:3). There were obtained 2.22 g (64%) of 4- [[6-(diethylamino)hexyl]oxy]benzaldehyde as a yellowish oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05106878uspto-grants-1992_04