反応 #307204

反応方程式

methyl 5-bromonicotinate

4-trifluoromethoxyphenylboronic acid

ethyl acetate

potassium fluoride

→

Methyl 5-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxylate

溶媒

ethanol

toluene

water

反応条件

後処理

1. 1
   温度under reflux overnight
2. 2
   workup.STIRRINGthe mixture was stirred
3. 3
   温度under reflux for a further 24 h
4. 4
   workup.STIRRINGthe mixture was stirred
5. 5
   温度under reflux for 20 h
6. 6
   洗浄washed with water and saturated aqueous sodium chloride solution
7. 7
   乾燥The organic phase was dried over magnesium sulphate
8. 8
   ろ過filtered
9. 9
   濃縮concentrated under reduced pressure
10. 10
    その他The residue was purified by means of column chromatography (silica gel, cyclohexane/dichloromethane 1:1→dichloromethane)

実験手順

A solution of 26 g (121 mmol) of methyl 5-bromonicotinate in toluene (220 ml) was admixed under argon at RT with 2.8 g (2.4 mmol) of tetrakis(triphenylphosphine)palladium, and then a solution of 30 g (146 mmol) of 4-trifluoromethoxyphenylboronic acid in ethanol (58 ml) was added. After adding 14 g (243 mmol) of potassium fluoride in water (58 ml), the mixture was stirred under reflux overnight, a further 0.70 g (0.61 mmol) of tetrakis(triphenylphosphine)palladium was added, and the mixture was stirred under reflux for a further 24 h. After adding another 1.4 g (1.2 mmol) of tetrakis(triphenylphosphine)palladium, the mixture was stirred under reflux for 20 h, and the reaction solution was admixed with ethyl acetate and washed with water and saturated aqueous sodium chloride solution. The organic phase was dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by means of column chromatography (silica gel, cyclohexane/dichloromethane 1:1→dichloromethane). Yield: 31 g (86% of theory)

出典