Реакция #417963
ord-4b5a523603fd4ce2a4d381c05c57e5fa
Уравнение реакции
Растворители
Условия реакции
Обработка
- 1Другоеcondensed at −78° C
- 2Температураthe reaction warmed to −45° C. for 2 hrs
- 3Другоеto evaporate
- 4workup.ADDITIONThe crude pot was then diluted in chloroform
- 5workup.ADDITION100 g of NH4Cl was added slowly
- 6ДругоеThe combines were taken up in a separatory funnel
- 7Промывкаwashed with water (3×)
- 8СушкаThe organic layer was dried over sodium sulfate
- 9Концентрированиеconcentrated in vacuo
- 10ДругоеThe resulting solid can be used without further purification
Методика
900 mL of ammonia was condensed at −78° C. 1 g of thinly shaven strips of sodium was added followed by 1.0 g of iron (III) nitrate nonahydrate. Upon disappearance of the deep blue color 25 g of thinly shaven strips of sodium was added. After 30 mins of stirring at −78° C., 50 g of 2,5-dichloroanisole was added as a solution in hexane (70 mL) dropwise and the reaction warmed to −45° C. for 2 hrs. Upon completion the ammonia was allowed to evaporate. The crude pot was then diluted in chloroform and 100 g of NH4Cl was added slowly. The combines were taken up in a separatory funnel and washed with water (3×) followed by brine (1×). The organic layer was dried over sodium sulfate and concentrated in vacuo. The resulting solid can be used without further purification. Yield: 99%.