反応 #1885005

反応方程式

1-naphthylboronic acid

4-bromo-2-nitrobiphenyl

potassium carbonate

→

4-naphth-1-yl-2-nitrobiphenyl

溶媒

water

THF

反応条件

後処理

1. 1
   その他degassed
2. 2
   温度the mixture is heated
3. 3
   温度under reflux for 17 h
4. 4
   温度After cooling
5. 5
   その他the organic phase is separated off
6. 6
   洗浄washed three times with 400 ml of water
7. 7
   乾燥once with 400 ml of saturated, aqueous sodium chloride solution, dried over magnesium sulfate
8. 8
   その他evaporated to dryness in vacuo in a rotary evaporator
9. 9
   その他The grey residue is recrystallised from hexane
10. 10
    ろ過The deposited crystals are filtered off with suction
11. 11
    洗浄washed with a little MeOH
12. 12
    その他dried in vacuo

実験手順

1.62 g (1.40 mmol) of Pd(PPh3)4 are added to a well-stirred, degassed suspension of 46 g (268 mmol) of 1-naphthylboronic acid, 71 g (255.3 mmol) of 4-bromo-2-nitrobiphenyl and 93 g (433.9 mmol) of potassium carbonate in a mixture of 700 ml of water and 700 ml of THF, and the mixture is heated under reflux for 17 h. After cooling, the organic phase is separated off, washed three times with 400 ml of water and once with 400 ml of saturated, aqueous sodium chloride solution, dried over magnesium sulfate and evaporated to dryness in vacuo in a rotary evaporator. The grey residue is recrystallised from hexane. The deposited crystals are filtered off with suction, washed with a little MeOH and dried in vacuo; yield: 83.1 g, 97.9% of theory; purity: 99.0% according to HPLC.

出典