Реакция #62850

ord-5ecc8e636b764733b716362d56ec77c5

Уравнение реакции

CN(C)CCN
N,N-dimethylethylenediamine
c1ccncc1
pyridine
CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCBr
3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl bromide
CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCNCCN(C)C
title compound
Выход 33.4%
CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCNCCN(C)C
N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenyl)-N',N'-dimethylethylenediamine
Выход 33.4%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture was heated
  2. 2
    Температураunder reflux for 2 h
  3. 3
    ЭкстракцияAfter extraction with n-hexane
  4. 4
    Промывкаby washing with water and concentration
  5. 5
    Другоеthe resulting reaction mixture
  6. 6
    workup.ADDITIONwas treated by alumina column chromatography

Методика

4.4 g of N,N-dimethylethylenediamine was dissolved in 40 ml of dioxane. 5 ml of pyridine was added to the solution. 17.6 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl bromide was added thereto and the mixture was heated under reflux for 2 h and poured in ice-water. After extraction with n-hexane followed by washing with water and concentration, the resulting reaction mixture was treated by alumina column chromatography to obtain 6 g (33%) of the title compound as a colorless oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04762829uspto-grants-1988_08