Реакция #63147

ord-ec1eade7d6bd4b7d8bf0561849d4cd2f

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthen recooled to -20°
  2. 2
    workup.WAITAfter 10 minutes at -15°
  3. 3
    Температураthe mixture was then heated
  4. 4
    Температураto reflux overnight
  5. 5
    Температураafter cooling the mixture to 15°
  6. 6
    workup.STIRRINGthe mixture was stirred vigorously in the presence of air
  7. 7
    Другоеremoval of the copper salts
  8. 8
    ДругоеThe aqueous phase was separated
  9. 9
    Экстракцияextracted with more ethyl acetate
  10. 10
    Промывкаthe combined organic extracts were washed successively with concentrated ammonium hydroxide, water and brine
  11. 11
    Сушкаdried (MgSO4)
  12. 12
    Другоеevaporated to an oil
  13. 13
    ДругоеThe product crystallized from ether/hexanes

Методика

A solution of 11.3 g (0.0436 mol) N-(1,1-dimethylethyl)-2-(methylthio)benzenesulfonamide in 300 ml tetrahydrofuran (THF) was treated with 60.5 ml (0.096 mol) 2M n-butyllithium in hexanes at -30° under a nitrogen atmosphere. The mixture was stirred for 1 hour at ambient temperature then recooled to -20° and treated with 8.3 g (0.0436 mol) of cuprous iodide (anhydrous). After 10 minutes at -15°, 4.9 ml (0.0438 mol) iodobenzene was added and the mixture was then heated to reflux overnight. Acetic acid (10 ml) was added after cooling the mixture to 15°, then 200 ml concentrated ammonium hydroxide plus 200 ml ethyl acetate was introduced and the mixture was stirred vigorously in the presence of air to facilitate removal of the copper salts. The aqueous phase was separated, extracted with more ethyl acetate and the combined organic extracts were washed successively with concentrated ammonium hydroxide, water and brine, then dried (MgSO4) and evaporated to an oil. The product crystallized from ether/hexanes to afford 10 g of material, m.p. 162°-165°.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04764204uspto-grants-1988_08