Реакция #1469683
ord-4bb8b3f580ed432a89f636d0bf30115f
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGThe yellow to orange reaction mixture is stirred for a further 15 hours
- 2Температураwithout being cooled
- 3workup.STIRRINGthe mixture is stirred thoroughly
- 4ДругоеThe phases are separated
- 5Экстракцияthe organic phase is extracted
- 6workup.STIRRINGby shaking with 300 ml of water
- 7Экстракцияthe aqueous phases are extracted with 300 ml of methylene chloride
- 8Сушкаthe combined organic phases are dried over sodium sulfate
- 9ФильтрацияThe solution is filtered
- 10workup.DISTILLATIONthe solvent is distilled off
- 11Другоеto give 75.0 g (=77% of theory) of crude product which
- 12ДругоеRecrystallization from methanol
Методика
57.0 g (0.30 mole) of n-octylbenzene are dissolved in 800 ml of carbon disulfide, the solution is cooled to 0° C., 66.5 g (0.50 mole) of aluminum chloride are added, and a solution of 40.0 g (0.30 mole) of phenylglyoxal and 50 ml of carbon disulfide are added dropwise at from 5° to 10° C., while stirring vigorously. The yellow to orange reaction mixture is stirred for a further 15 hours without being cooled, after which it is poured carefully onto 1 l of semiconcentrated ice-cold hydrochloric acid, and the mixture is stirred thoroughly. The phases are separated, the organic phase is extracted by shaking with 300 ml of water, the aqueous phases are extracted with 300 ml of methylene chloride, and the combined organic phases are dried over sodium sulfate. The solution is filtered and the solvent is distilled off to give 75.0 g (=77% of theory) of crude product which has a melting range of 85°-89° C. and is 95% pure according to gas chromatography. Recrystallization from methanol gives analytically pure 4'-n-octylbenzoin.