Реакция #2006464

ord-c5171f7de3ee4505b82cd91675132588

Уравнение реакции

C=CCC(CC=C)(C(=O)OCC)C(=O)OCC
diethyl diallylmalonate
[C-]#N.[Na+]
sodium cyanide
CS(C)=O
DMSO
C=CCC(CC=C)C(=O)OCC
702
Выход 78.1%
C=CCC(CC=C)C(=O)OCC
4-Carbethoxy-1,6-heptadiene
Выход 78.1%

Реагенты

Нет

Растворители

Условия реакции

Температура
160°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter being cooled to r.t.
  2. 2
    Экстракцияthe product was extracted into hexane (4×100 mL)
  3. 3
    ДругоеAfter evaporation of the solvent at reduced pressure
  4. 4
    workup.DISTILLATIONthe residue was distilled (42-43° C./1 Torr)

Методика

A mixture of diethyl diallylmalonate (701; 50 g, 208 mmol), sodium cyanide (20.7 g, 422 mmol) and DMSO (166 mL) was heated at 160° C. for 6 h. After being cooled to r.t., the mixture was added to 400 mL of water and the product was extracted into hexane (4×100 mL). After evaporation of the solvent at reduced pressure, the residue was distilled (42-43° C./1 Torr) to give 27.34 g (78%) of 702 as a colorless liquid. 1H NMR (400 MHz, CDCl3) δ 5.80-5.70 (m, 2H, 2 CH═CH2), 5.10-5.02 (m, 4H, 2 CH═CH2), 4.14 (q, 2H, J=7.2 Hz, OCH2), 2.54-2.48 (m, 1H, CH), 2.41-2.34, 2.29-2.23 (2m, 4H, 2CH2), 1.25 (t, J=7.2 Hz, 3H, CH3).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08168583B2uspto-grants-2012_05