Реакция #65572
ord-01f89205b7bd469b9be2af90e59305c7
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1КонцентрированиеThe mixture is concentrated
- 2workup.DISSOLUTIONthe residue is dissolved in ethyl ether
- 3ПромывкаThe solution is washed with diluted hydrochloric acid, aqueous sodium hydrogencarbonate solution and brine
- 4СушкаThe organic layer is dried over sodium sulfate
- 5Фильтрацияfiltered off
- 6workup.DISTILLATIONThe filtrate is distilled away
- 7Другоеthe resuling residue is crystallized
Методика
To a solution of 0.82 g of 2-tert-butyl-6-methylaniline in pyridine is added a solution of 1.2 g of N-methyl-N-(2-phenylcyclohexyl)carbamoylchloride in dichloromethane dropwise. The mixture is stirred at room temperature until starting compounds disappear on TLC. The mixture is concentrated and the residue is dissolved in ethyl ether. The solution is washed with diluted hydrochloric acid, aqueous sodium hydrogencarbonate solution and brine. The organic layer is dried over sodium sulfate and filtered off. The filtrate is distilled away and the resuling residue is crystallized to give N-(2-tert-butyl-6-methylphenyl)-N'-methyl-N'-(2-phenylcyclohexyl)urea.