Реакция #90558

Уравнение реакции

3,5-dibromo pyridine

isopropyl magnesium chloride

Hexafluoroacetone

→

2-(5-bromopyridin-3-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol

Растворители

THF

Условия реакции

Обработка

1. 1
   workup.STIRRINGcontinued stirring for another 2 h
2. 2
   ДругоеAfter completion of the starting materials, the reaction was quenched with saturated ammonium chloride solution
3. 3
   ДругоеThe organic layer was separated
4. 4
   Экстракцияaqueous phase was extracted again with diethyl ether
5. 5
   Сушкаthe combined organic layer was dried over sodium sulphate
6. 6
   Концентрированиеconcentrated

Методика

To a stirred solution of 3,5-dibromo pyridine 257 (1.09 g, 4.60 mmol) in dry THF cooled to 0° C., was added isopropyl magnesium chloride (2.4 mL, 4.8 mmol) drop wise while stirring for 10 min. Hexafluoroacetone (CF3—CO—CF3) 244 was added to the resulting reaction and continued stirring for another 2 h. After completion of the starting materials, the reaction was quenched with saturated ammonium chloride solution. The organic layer was separated and aqueous phase was extracted again with diethyl ether, the combined organic layer was dried over sodium sulphate and concentrated to get the crude 2-(5-bromopyridin-3-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol 258. The crude was purified through silica gel by using 100-200 mesh silica gel by eluting the compound at 20:5 ethyl acetate in hexane as thick oil of compound 258.

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