تفاعل #85154
ord-bd86b2b2b4b94a849ac3e96ea4f9d0ad
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىthe reaction was subsequently terminated by addition of 10 ml of methanol
- 2workup.ADDITIONThe reaction mixture was diluted with 30 ml of aqueous 20% strength sodium potassium tartrate solution and 30 ml of aqueous buffer solution (pH 7)
- 3workup.STIRRINGstirred vigorously at room temperature overnight
- 4أخرىThe phases were separated
- 5استخلاصthe aqueous phase was extracted three times with dichloromethane
- 6تجفيفThe combined organic phases were dried over magnesium sulphate
- 7ترشيحfiltered
- 8أخرىthe solvent was removed under reduced pressure
الإجراء التجريبي
At 0° C., 26.7 ml (26.7 mmol) of diisobutylaluminum hydride (1M in dichloromethane) were slowly added dropwise to a solution of 1.89 g (10.7 mmol) of methyl 1-(trifluoromethyl)cyclopropanecarboxylate in 10 ml of dichloromethane. The mixture was then stirred at 0° C. for another 2 h and the reaction was subsequently terminated by addition of 10 ml of methanol. The reaction mixture was diluted with 30 ml of aqueous 20% strength sodium potassium tartrate solution and 30 ml of aqueous buffer solution (pH 7) and stirred vigorously at room temperature overnight. The phases were separated and the aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The crude product corresponded to the title compound. Yield: 0.96 g (64% of theory)