反応 #165463

反応方程式

2-fluoropyridine

water

4-bromobenzyl alcohol

potassium tert-butoxide

→

title compound

収率 99.0%

2-(4-Bromo-benzyloxy)-pyridine

収率 99.0%

溶媒

ethyl acetate

N,N-dimethyl formamide

反応条件

後処理

1. 1
   workup.STIRRINGwas further stirred for 30 minutes at 65° C
2. 2
   その他was allowed to room temperature
3. 3
   その他liquid separation
4. 4
   抽出The aqueous layer was further extracted with ethyl acetate (twice)
5. 5
   洗浄washed with water (3 times) and sodium chloride water (once),
6. 6
   乾燥dried over anhydrous magnesium sulfate
7. 7
   ろ過filtered
8. 8
   濃縮The filtrate was concentrated under a reduced pressure
9. 9
   workup.ADDITIONDiethyl ether was added to the residue, which
10. 10
    濃縮was concentrated under a reduced pressure

実験手順

To a solution of 4-bromobenzyl alcohol (25 g, 130 mmol) in N,N-dimethyl formamide (125 mL) was added potassium tert-butoxide (15.8 g, 141 mmol) at room temperature, which was stirred at 54° C. for 10 minutes. To this reaction solution was added 2-fluoropyridine (15 mL, 154 mmol) at from 40° C. to 58° C., which was further stirred for 30 minutes at 65° C. The reaction solution was allowed to room temperature, water and ethyl acetate were added, and liquid separation was carried out. The aqueous layer was further extracted with ethyl acetate (twice). The ethyl acetate layers were combined, washed with water (3 times) and sodium chloride water (once), dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure. Diethyl ether was added to the residue, which was concentrated under a reduced pressure to obtain the title compound (34 g) as a crude product.

出典