반응 #543618

반응 방정식

3-fluoro anisole

n-BuLi

bromine

→

2-Bromo-3-fluoro-anisole

용매

THF

반응 조건

후처리

1. 1
   온도while maintaining the temperature at around −70° C
2. 2
   온도The mixture was warmed to r.t.
3. 3
   workup.STIRRINGstirred overnight
4. 4
   기타The mixture was quenched with water
5. 5
   workup.ADDITIONdiluted with ether (500 mL)
6. 6
   기타partitioned between water/ether (1/1 300 mL)
7. 7
   추출The water layer was back extracted with ether (250 mL)
8. 8
   기타the combined organic fractions were dried
9. 9
   여과filtered
10. 10
    농축concentrated
11. 11
    workup.DISTILLATIONThe dark residue was distilled under house vacuum (product 115–130° C.)
12. 12
    기타to recover about 13.8 g of the product as a gray oil (57%)

실험 절차

The 3-fluoro anisole (15 g, 119 mmol) was placed in THF (300 mL) and cooled to about −78° C., and then n-BuLi (89 mL 1.6 M in hexanes) was added while maintaining the temperature at around −70° C. The mixture was stirred for about 15 minutes, and bromine (18.9 g, 119 mmol) was added over 10 minutes. The mixture was warmed to r.t. and stirred overnight. The mixture was quenched with water, diluted with ether (500 mL) and partitioned between water/ether (1/1 300 mL). The water layer was back extracted with ether (250 mL), and the combined organic fractions were dried, filtered and concentrated. The dark residue was distilled under house vacuum (product 115–130° C.) to recover about 13.8 g of the product as a gray oil (57%).

출처