Реакция #1005938

Уравнение реакции

1-(4-chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazole

iodine

→

1-(4-chlorophenyl)-3-[(Z)-3-iodobut-2-enoxy]pyrazole

Растворители

methylene chloride

Условия реакции

Обработка

1. 1
   ДругоеAfter removal of the solvents in vacuo the crude product
2. 2
   workup.DISSOLUTIONwas dissolved in 200 ml MTBE
3. 3
   workup.ADDITION100 ml 20% aqueous potassium fluoride solution have been added
4. 4
   workup.STIRRINGthe mixture was stirred for 2 h at ambient temperature
5. 5
   ДругоеThe aqueous layer was separated
6. 6
   Экстракцияextracted with 20 ml methyl-tert.-butyl ether twice
7. 7
   ПромывкаThe combined organic phases have been washed twice with 20 ml of water each,
8. 8
   Сушкаdried with sodium sulfate
9. 9
   Другоеthe solvents were removed in vacuo
10. 10
    ДругоеThe crude product (7.2 g) has been purified by chromatography on 50 g silica with methyl-tert.-butylether/hexane (1:20)

Методика

To 10.0 g (18.6 mmol) 1-(4-chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazole in 100 ml methylene chloride have been added 4.7 g (18.6 mmol) iodine at ambient temperature with stirring which was continued for 3 h. After removal of the solvents in vacuo the crude product was dissolved in 200 ml MTBE. 100 ml 20% aqueous potassium fluoride solution have been added and the mixture was stirred for 2 h at ambient temperature. The aqueous layer was separated and extracted with 20 ml methyl-tert.-butyl ether twice. The combined organic phases have been washed twice with 20 ml of water each, dried with sodium sulfate, and the solvents were removed in vacuo. The crude product (7.2 g) has been purified by chromatography on 50 g silica with methyl-tert.-butylether/hexane (1:20). Yield 5.9 g, melting point 75-77° C.

Источник