Реакция #2307969

ord-bd2db1b60b024ea392edcc4699afbc79

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter completion of the reaction
  2. 2
    Другоеthe 3-chlorobenzoicacid (by-product) was removed
  3. 3
    Фильтрацияby filtering the product
  4. 4
    Другоеthe residual 3-chlorobenzoicacid was removed
  5. 5
    Промывкаby washing 2 times with saturated sodium sulfite aqueous solution, 1 time with saturated sodium bicarbonate aqueous solution, 1 time with saturated sodium chloride aqueous solution, and 1 time with distilled water
  6. 6
    СушкаNext, the product was dried with magnesium sulfate, and chloroform
  7. 7
    Другоеwas removed under reduced pressure
  8. 8
    Другоеdried for 1 day

Методика

30 g of 4-acetoxy styrene and 1 L of chloroform were added into a 2 L reactor, and was stirred and cooled in iced water. 47 g of 3-chloroperoxybenzoicacid were added into the cooled solution, and the reaction was carried out at room temperature for 24 hours. After completion of the reaction, the 3-chlorobenzoicacid (by-product) was removed by filtering the product, and then the residual 3-chlorobenzoicacid was removed by washing 2 times with saturated sodium sulfite aqueous solution, 1 time with saturated sodium bicarbonate aqueous solution, 1 time with saturated sodium chloride aqueous solution, and 1 time with distilled water. Next, the product was dried with magnesium sulfate, and chloroform was removed under reduced pressure, and then the product was vacuum dried for 1 day to obtain 27.6 g of the pure 4-acetoxy styreneoxide.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07368219B2uspto-grants-2008_05