Реакция #54508
ord-e13f36d1f3a648878cd8800005964c27
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.DISSOLUTIONto dissolve the organic matter and air
- 2Другоеwas then bubbled through the solution for 3 hours
- 3ЭкстракцияThe resulting solution was extracted with 100 parts petroleum ether (twice),
- 4Экстракцияre-extracted with diethylether
- 5ЭкстракцияThe ether extract
- 6Промывкаwas washed with saturated sodium chloride
- 7Сушкаdried over magnesium sulfate
- 8Другоеevaporated
- 9Фильтрацияfiltered
- 10ДругоеThe filtrate was evaporated to dryness
- 11Другоеthe residue triturated with petroleum ether
Методика
Four parts of crude ethyl 2-[(2-methylphenyl)acetyl]tetradecanoate obtained in Example 3 was combined with 12 parts of cold concentrated sulfuric acid and stirred at room temperature for 66 hours. The mixture was poured into ice water and made slightly basic by the addition of 50% aqueous sodium hydroxide. Enough ethanol was added to dissolve the organic matter and air was then bubbled through the solution for 3 hours. The resulting solution was extracted with 100 parts petroleum ether (twice), acidified with hydrochloric acid and re-extracted with diethylether. The ether extract was washed with saturated sodium chloride, dried over magnesium sulfate and evaporated. The residue was taken up in acetonitrile and filtered. The filtrate was evaporated to dryness and the residue triturated with petroleum ether to give 0.2 g of 2-dodecyl-3-hydroxy-5-methyl-1,4-napthoquinone, m.p. 92°-93° C.