Реакция #432377

ord-0e364f3de92147eebb472fe12c1927e9

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted
  2. 2
    workup.STIRRINGby shaking
  3. 3
    КонцентрированиеThe dried organic phase is concentrated
  4. 4
    ДругоеThe residue is recrystallized from 2-methoxy-ethanol
  5. 5
    Другоеgiving red-orange crystals

Методика

4-(4,6-Bis-trichloromethyl-s-triazin-2-yl)benzoylchloride (15.4 pbw) are added dropwise with stirring at 10° C. to 5.2 pbw of 1,3,3-trimethyl-2-methylene-indoline and 10.6 pbw of triethylamine in 140 pbw of anhydrous toluene. The mixture is stirred for 3 hours at room temperature. It is then admixed with 100 pbw of water and 200 pbw of ether and extracted by shaking. The dried organic phase is concentrated. The residue is recrystallized from 2-methoxy-ethanol, giving red-orange crystals.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05055579uspto-grants-1991_10