Реакция #10033

ord-38c716d7c7e943708a6e3647fcb2217f

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture is cooled at about 5° C.
  2. 2
    ДругоеAfter separation of the phases
  3. 3
    Экстракцияthe aqueous layer is extracted with chlorobenzene (90 ml)
  4. 4
    Промывкаthe combined organic layers are washed with water (100 ml)
  5. 5
    Другоеevaporated under reduced pressure
  6. 6
    workup.ADDITIONThe obtained residue (116.9 g, containing, according to HPLC assay, 104.8 g of pure product, 88% molar yield)
  7. 7
    Другоеis used for the next step of the synthesis without any further purification

Методика

To a solution of N-methylformanilide (100 g), butyl vinyl ether (74.12 g) in 85 ml of clorobenzene under stirring at 5° C., a solution of bis-trichloromethylcarbonate (87.84 g) in 170 ml of clorobenzene is added dropwise in 2 hours. The reaction mixture is kept under stirring at room temperature overnight. The mixture is cooled at about 5° C. and the pH is corrected to about 7 by adding sodium hydroxide 15% aqueous solution (348 ml). After separation of the phases, the aqueous layer is extracted with chlorobenzene (90 ml) and the combined organic layers are washed with water (100 ml) and evaporated under reduced pressure. The obtained residue (116.9 g, containing, according to HPLC assay, 104.8 g of pure product, 88% molar yield) is used for the next step of the synthesis without any further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091382B2uspto-grants-2006_08