Реакция #6629

ord-906733f298d349598a10f27ec82e8d53

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThis solution was refluxed
  2. 2
    ДругоеThe supernatant organic layer was decanted
  3. 3
    Экстракцияthe syrupy residue extracted with 3×50ml ether
  4. 4
    Промывкаwashed with water, saturated NaHCO3 and saturated NaCl solutions
  5. 5
    Сушкаdried (MgSO4)
  6. 6
    ДругоеSolvent was removed in vacuo
  7. 7
    workup.DISTILLATIONthe residue purified by kugelrohr distillation (80 degrees C., 0.5mm)

Методика

To a solution of 15.48g (86.824 mmol) of phenyl-3-methylbut-2-enylsulfide (Compound 60) in 160ml benzene were added successively 12.6g (88.767mmol) of phosphorus pentoxide and 11 ml of 85% phosphoric acid. This solution was refluxed with vigorous stirring under argon for 20 hours, then cooled to room temperature. The supernatant organic layer was decanted and the syrupy residue extracted with 3×50ml ether. Organic fractions were combined and washed with water, saturated NaHCO3 and saturated NaCl solutions and then dried (MgSO4). Solvent was removed in vacuo and the residue purified by kugelrohr distillation (80 degrees C., 0.5mm) to give the title compound as a pale yellow oil. PMR (CDCl3) :& 1.30 (6H, s), 1.90-1.95 (2H, m), 2.95-3.00 (2H, m), 6.96-7.00 (2H, m), 7.04-7.07 (1H, m), 7.30-7.33 (1H, m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05248777uspto-grants-1993_09