反应 #2271668
ord-5b33fe3929024bc59431748dcaa202b6
反应方程式
6-fluoro-3-(4-piperidinyl)-1,2 benzisoxazole hydrochloride
K2CO3
1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone
dimethylformamide
→
1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]-ethanone
收率 58.6%
反应物
试剂
无
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1萃取the aqueous mixture was extracted with ethyl acetate
- 2洗涤The ethyl acetate was washed (water)
- 3干燥dried (MgSO4)
- 4浓缩concentrated
- 5其他to afford a moist solid
- 6其他Recrystallization (twice) from ethyl alcohol
实验过程
A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2 benzisoxazole hydrochloride (5.1 g, 20 mmol). K2CO3 (5.2 g, 40 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (5.3 g, 22 mmol), and dimethylformamide (60 ml) was heated at 90° C. for 16 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed (water), dried (MgSO4) and concentrated to afford a moist solid. Recrystallization (twice) from ethyl alcohol afforded 5.0 g (58%) of 1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]-ethanone as a beige solid, m.p.=118°-120° C.