Реакция #1857542

ord-b37ba3fbf1c34340a361306fe0dd4206

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added carefully
  2. 2
    ЭкстракцияThe mixture was extracted with MTBE (3×)
  3. 3
    Промывкаthe combined organic phases were washed with water
  4. 4
    Другоеdried
  5. 5
    Другоеevaporated

Методика

DMSO (150 mL) was added dropwise to a mixture of sodium hydride (22 g) in THF (600 mL). After completion of the addition a solution of trimethylsulfonium iodide (171 g) in DMSO (300 mL) was added slowly at 5° C. whereupon a solution of 1-[2-chloro-4-(4-chlorophenoxy)phenyl]ethanone (107 g) in DMSO (300 mL) was added carefully. The mixture was stirred for 1 h at room temperature and dil. NH4Cl solution was added. The mixture was extracted with MTBE (3×) and the combined organic phases were washed with water, dried and evaporated to obtain the desired compound that was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09247746B2uspto-grants-2016_02