Реакция #158335

Уравнение реакции

ammonium chloride

3,4-Dichlorophenylmagnesium bromide

6-[3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl]hex-5-ynal

3,4-Dichlorophenylmagnesium bromide

→

title compound

1-(3,4-dichlorophenyl)-6-[3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl]hex-5-yn-1-ol

Растворители

THF

Условия реакции

Обработка

1. 1
   Температураcooling
2. 2
   workup.STIRRINGthe mixture was stirred for 1 hr under ice-
3. 3
   Температураcooling
4. 4
   Экстракцияthe mixture was extracted with ethyl acetate
5. 5
   ПромывкаThe extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
6. 6
   Сушкаdried over anhydrous sodium sulfate
7. 7
   Другоеthe solvent was evaporated under reduced pressure
8. 8
   ДругоеThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Методика

3,4-Dichlorophenylmagnesium bromide (0.5 M THF solution, 13 mL) was added dropwise to a mixture of 6-[3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl]hex-5-ynal (900 mg) in THF (32 mL) at −78° C., and the mixture was stirred for 1 hr under ice-cooling and at room temperature for 14 hr. 3,4-Dichlorophenylmagnesium bromide (0.5M THF solution, 13 mL) was added to the reaction mixture under ice-cooling, and the mixture was stirred for 1 hr under ice-cooling. Saturated aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (349 mg).

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