反应 #1519078

ord-4f1613edb89d4506a46a5ac1c2856aa0

反应方程式

CC1=CC(=C(C#N)C#N)C=C(C)O1
(2,6-dimethyl-4H-pyran-4-ylidene)malononitril
CCCCC(CC)CN
2-ethyl-1-hexylamine
CCCCC(CC)CN1C(C)=CC(=C(C#N)C#N)C=C1C
1-N-(2-ethylhexyl)-4-dicyanomethylene-2,6-dimethyl-1,4-dihydropyridine

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Removal of the excess of ethyl-1-hexylamine at reduced pressure
  2. 2
    workup.WAITleft a solid which
  3. 3
    其他was recrystallized from 15 ml EtOAc/MeOH 2/1 yielding 0.45 g (55%) of 1-N-(2-ethylhexyl)-4-dicyanomethylene-2,6-dimethyl-1,4-dihydropyridine

实验过程

A solution of 0.5 g (2.9 mmol) of (2,6-dimethyl-4H-pyran-4-ylidene)malononitril in 7.6 ml (6 g, 46.4 mmol) 2-ethyl-1-hexylamine was refluxed for 1 h under nitrogen. Removal of the excess of ethyl-1-hexylamine at reduced pressure left a solid which was recrystallized from 15 ml EtOAc/MeOH 2/1 yielding 0.45 g (55%) of 1-N-(2-ethylhexyl)-4-dicyanomethylene-2,6-dimethyl-1,4-dihydropyridine.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07611696B2uspto-grants-2009_11