Реакция #2481496

ord-7bca85b58ba14edd93d1a42b3fda365b

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAfter the reaction mixture was concentrated under reduced pressure, 180 ml of concentrated hydrochloric acid, 100 ml of water, and 300 ml of diethyl ether
  2. 2
    workup.ADDITIONwere added to the residue
  3. 3
    Экстракцияthe organic substances were extracted with 500 ml of ethyl acetate
  4. 4
    ПромывкаThe organic layer was washed with water
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    Другоеwas removed from the obtained oily products

Методика

82 g of ammonium acetate and 6.7 g of sodium cyanoborohydride were added to a solution containing 21 g of 3-(4-chlorophenoxy)-2-butanone dissolved in 500 ml of methanol, and the reaction mixture was stirred for 20 hours at room temperature. After the reaction mixture was concentrated under reduced pressure, 180 ml of concentrated hydrochloric acid, 100 ml of water, and 300 ml of diethyl ether were added to the residue. The obtained water layer was alkalified using a 5% aqueous solution of sodium hydroxide, and then the organic substances were extracted with 500 ml of ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. A fraction possessing a low boiling point was removed from the obtained oily products to afford 18 g (yield 86%) of the desired product.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05811424uspto-grants-1998_09