Реакция #969846

ord-2b2913496c594ea09edbc4391bb9c9aa

Растворители

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеevaporated
  2. 2
    workup.DISSOLUTIONThe mixture was redissolved in methanol
  3. 3
    Фильтрацияfiltered through celite,
  4. 4
    Концентрированиеconcentrated
  5. 5
    Другоеpurified with SiO2 chromatography
  6. 6
    Промывкаeluted with CH3OH/CH2Cl2/HCOOH 37.5:250:1 to 50:250:1)

Методика

5.0 g (19.2 mmol) of 4-bromo-1-methoxy-1-oxobutane-2-sulfonic acid in 100 ml of THF was added 3.0 ml of thioacetic acid and 9.0 ml of DIPEA in 100 ml of THF. The mixture was stirred overnight then refluxed at 70° C. for 1 hr, evaporated and co-evaporated with 3×100 ml of water after neutralized to pH 7 with NaHCO3. The mixture was redissolved in methanol, filtered through celite, concentrated and purified with SiO2 chromatography eluted with CH3OH/CH2Cl2/HCOOH 37.5:250:1 to 50:250:1) to afford 4.4 g (90% yield) of the title compound. 1H NMR (D2O) 3.95 (dd, 1H, J=4.1, 10.3 Hz), 3.83 (s, 3H), 3.74 (m, 2H), 3.22 (dd, 2H, J=7.4, 14.9 Hz), 2.39 (s, 3H); 13C NMR 203.88, 172.91, 67.32, 56.17, 29.04, 20.61; MS m/z−254.8 (M−H)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08236319B2uspto-grants-2012_08