反应 #943987

反应方程式

6,7-dimethoxy-1-tetralone

1-(2-(4-bromophenoxy)ethyl)pyrrolidine

n-butyllithium

→

product

收率 36.2%

1-{2-[4-(6,7-Dimethoxy-3,4-dihydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine

收率 36.2%

溶剂

THF

THF

ether

反应条件

后处理

1. 1
   温度to maintain a clear solution
2. 2
   其他the temperature below −70° C
3. 3
   其他the temperature below −70° C
4. 4
   workup.STIRRINGAfter stirring for 2.5 hours at −78° C.
5. 5
   其他the reaction was quenched by addition of 100 ml of 2N HCl
6. 6
   温度to warm to room temperature
7. 7
   workup.ADDITIONthe pH was adjusted to 7 by addition of 5N NaOH
8. 8
   其他The Et2O layer was separated
9. 9
   萃取the aqueous layer was extracted 2 times with EtOAc
10. 10
    干燥The combined Et2O/EtOAc layers were dried over Na2SO4
11. 11
    其他evaporated
12. 12
    其他to give 9 g of crude product, which
13. 13
    其他was purified on 400 g of silica gel eluting with 95/5 CH2Cl2/MeOH
14. 14
    其他to remove

实验过程

A solution of 6.75 g (0.025 moles) of 1-(2-(4-bromophenoxy)ethyl)pyrrolidine in 250 ml of ether was cooled to −78° C. under N2. Several ml of THF were added to maintain a clear solution. 16.7 ml of 1.6 M n-butyllithium was added dropwise keeping the temperature below −70° C. After stirring at −78° C. for 1 hour, a solution of 5 g (0.024 moles) of 6,7-dimethoxy-1-tetralone in 25 ml of THF was added dropwise during 1 hour keeping the temperature below −70° C. After stirring for 2.5 hours at −78° C., the reaction was quenched by addition of 100 ml of 2N HCl. The reaction was allowed to warm to room temperature and the pH was adjusted to 7 by addition of 5N NaOH. The Et2O layer was separated and the aqueous layer was extracted 2 times with EtOAc. The combined Et2O/EtOAc layers were dried over Na2SO4 and evaporated to give 9 g of crude product, which was purified on 400 g of silica gel eluting with 95/5 CH2Cl2/MeOH to remove starting tetralone then with 85/15 CH2Cl2/MeOH to give 3.3 g of product.

来源