Реакция #631992
ord-d71cbefdad454d5a89446f851b291fce
Уравнение реакции
3-(dodecylthio)-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone
EtOH
→
title compound
Выход 38.0%
3-(dodecylsulfinyl)-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone
Выход 38.0%
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Другоеwas brought to room temperature
- 2Экстракцияtitle compound extracted (ether/brine)
- 3ПромывкаThe organic phase was washed with aqueous NaHSO3, H2O, saturated aqueous NaHCO3
- 4Сушкаbrine, dried over Na2SO4
- 5Концентрированиеconcentrated
Методика
A solution of 3-(dodecylthio)-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone (2.00 g; 5.10 mmol) in MeOH (20 ml) was added at 0° C. to a solution of NaIO4 (1.14 g, 5.30 mmol) in H2O (11 ml). The temperature was brought to room temperature and EtOH (30 ml) was added. The suspension was stirred for 15 h and title compound extracted (ether/brine). The organic phase was washed with aqueous NaHSO3, H2O, saturated aqueous NaHCO3, then brine, dried over Na2SO4, and concentrated. (16.2 g). Flash chromatography (cyclohexane/ethyl acetate=7:3, then 1:1) on SiO2 (40 g) afforded 803 mg of the title compound (38%).