Реакция #552205
ord-0e30df148e214556a028d39347442c01
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Температура
-5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Экстракцияextracted with ether
- 2СушкаThe extract was dried (MgSO4)
- 3Другоеthe solvent was evaporated
- 4Другоеchromatographed on silica gel
- 5workup.ADDITIONv:v mixture of tetrahydrofuran, ethyl acetate and hexane as eluent
Методика
15.6 g of 1E was mixed with 150 ml of THF and 11.3 g of N,N-diisopropylethylamine. The mixture was cooled to -5° C. and 9.1 g of methyl chloroformate was added drop-by-drop to the stirred mixture, stirred at 0° C. for two hours, then poured over ice water and extracted with ether. The extract was dried (MgSO4) and the solvent was evaporated. The residue was column chromatographed on silica gel, using a 1:4:20 v:v:v mixture of tetrahydrofuran, ethyl acetate and hexane as eluent, to give 2-(2,3-dihydro-2,4-dimethylbenzofuran-7-yl)hydrazinecarboxylic acid methyl ester (1F), as a tan solid, m.p.: 90°-92° C.