Реакция #411759

ord-4ce72148170c471da0fadc0f68790a20

Уравнение реакции

C=CCCC(=O)C1CCCN1C(=O)C(=O)C(C)(C)CC
3,3-dimethyl-1-(2-pent-4-enoylpyrrolidinyl)pentane-1,2-dione
Brc1ccc(OCc2ccccc2)cc1
4-benzyloxybromobenzene
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri(orthotolyl)phosphine
CCC(C)(C)C(=O)C(=O)N1CCCC1C(=O)CCC=Cc1ccc(OCc2ccccc2)cc1
3,3-dimethyl-1-(2-{5-[4-(phenylmethoxy)phenyl]pent-4-enoyl}pyrrolidinyl)pentane-1,2-dione
Выход 60.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe mixture was concentrated in vacuo
  2. 2
    Другоеpurified on a silica gel column
  3. 3
    Промывкаeluting with a gradient from 10% ethyl acetate/hexane to 20% ethyl acetate/hexane

Методика

A solution of 3,3-dimethyl-1-(2-pent-4-enoylpyrrolidinyl)pentane-1,2-dione (1.73 g; 6.20 mmol), 4-benzyloxybromobenzene (1.80 g; 6.83 mmol), palladium (II) acetate (70 mg; 0.31 mmol), and tri(orthotolyl)phosphine (380 mg; 1.24 mmol) in triethylamine (23 ml) was refluxed overnight. The mixture was concentrated in vacuo and purified on a silica gel column, eluting with a gradient from 10% ethyl acetate/hexane to 20% ethyl acetate/hexane, to obtain 1.72 g (60%) of 3,3-dimethyl-1-(2-{5-[4-(phenylmethoxy)phenyl]pent-4-enoyl}pyrrolidinyl)pentane-1,2-dione as a yellow oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06218424B1uspto-grants-2001_04