Реакция #1321
ord-2fe08cc9e6c748808fe5a8679bdd3bfb
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Концентрированиеconcentrated in vacuo
- 2Другоеpartitioned between 200 ml of water and 250 ml of ethyl ether
- 3Другоеthe layers were separated
- 4ПромывкаThe aqueous phase was washed with 2×150 ml-portions of ethyl ether
- 5Промывкаwashed once with 75 ml of brine solution
- 6Сушкаdried over MgSO4
- 7Фильтрацияfiltered
- 8Концентрированиеconcentrated in vacuo to a yellow solid
- 9ДругоеPurification by flash chromatography (silica, 10% ethyl acetate in hexane)
Методика
To a suspension of 23.38 g (94.2 mmol) of 6-iodonicotinic acid in 100 ml of dichloromethane was added a solution of 19.86 g (103.6 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride in 250 ml of dichloromethane. To this suspension was added 12.40 g (15.8 ml, 269.3 mmol) of ethanol (95%) and 1.15 g (9.4 mmol) of 4-dimethylaminopyridine. The resulting solution mixture was then heated at 50° C. in an oil bath for 24.5 hours, concentrated in vacuo, partitioned between 200 ml of water and 250 ml of ethyl ether, and the layers were separated. The aqueous phase was washed with 2×150 ml-portions of ethyl ether. All organic phases were combined, washed once with 75 ml of brine solution, dried over MgSO4, filtered and concentrated in vacuo to a yellow solid. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) yielded the title compound as a white solid.