Реакция #1519080

ord-185f83d30d51415380fa6dedfd0b8776

Уравнение реакции

CC1=CC(=C(C#N)C#N)C=C(C)O1
(2,6-dimethyl-4H-pyran-4-ylidene)malononitril
NCCCOCCOCCOCCCN
4,7,10-trioxa-1,13-tridecanediamine
CC1=CC(=C(C#N)C#N)C=C(C)N1CCCOCCOCCOCCCN1C(C)=CC(=C(C#N)C#N)C=C1C
2-{1-[3-(2-{2-[3-(4-dicyanomethylene-2,6-dimethyl-4H-pyridin-1-yl)-propoxy]-ethoxy}-ethoxy)-propyl]-2,6-dimethyl-1H-pyridin-4-ylidene}-malononitrile

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеRemoval of the acetonitrile
  2. 2
    workup.WAITleft a brown residue which
  3. 3
    Другоеwas recrystallized from 25 ml methanol and 10 ml ethyl acetate yielding 0.68 g (43%) of 2-{1-[3-(2-{2-[3-(4-dicyanomethylene-2,6-dimethyl-4H-pyridin-1-yl)-propoxy]-ethoxy}-ethoxy)-propyl]-2,6-dimethyl-1H-pyridin-4-ylidene}-malononitrile

Методика

A solution of 0.52 g (3 mmol) of (2,6-dimethyl-4H-pyran-4-ylidene)malononitril and 0.3 ml (1.5 mmol) of 4,7,10-trioxa-1,13-tridecanediamine in 6 ml of acetontrile was heated to 90° C. for 70 h under nitrogen. Removal of the acetonitrile left a brown residue which was recrystallized from 25 ml methanol and 10 ml ethyl acetate yielding 0.68 g (43%) of 2-{1-[3-(2-{2-[3-(4-dicyanomethylene-2,6-dimethyl-4H-pyridin-1-yl)-propoxy]-ethoxy}-ethoxy)-propyl]-2,6-dimethyl-1H-pyridin-4-ylidene}-malononitrile.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07611696B2uspto-grants-2009_11