Реакция #64016
ord-e0c0568465984b42829b79ad0df936eb
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеis removed under reduced pressure
- 2ДругоеThe residual dark solid is collected
- 3Промывкаwashed sequentially with acetonitrile and ether
- 4ДругоеCrystallization from ethyl acetate
- 5Другоеgave 9.0 g (14%) of isomer A (3: R=4-Cl, n=15), melting at 100°-102° C.
Методика
A solution of 32.8 g (0.131 mol) of 1-(4-chlorophenyl)-N-methyl-2-(1H-1,2,4-triazol-1-yl)ethanimine N-oxide (1: R=4-Cl) [prepared by reacting 2-(1H-1,2,4-triazol-1-yl)-4'-chloroacetophenone (35.38 g, 0.160 mol) with N-methylhydroxylamine hydrochloride (20.0 g, 0.240 mol) and NaHCO3 (20.12 g, 0.240 mol) in 500 ml ethanol] and 62.8 ml (0.196 mol) of 1-octadecene (2: n=15) in 400 ml toluene is refluxed for 48 hours under a nitrogen atmosphere. Upon cooling to room temperature the solvent is removed under reduced pressure. The residual dark solid is collected and washed sequentially with acetonitrile and ether. Crystallization from ethyl acetate gave 9.0 g (14%) of isomer A (3: R=4-Cl, n=15), melting at 100°-102° C.