反应 #1876813

ord-5820225fe8974a7692d95ff7a8e72a7a

反应方程式

CCOc1ccc(Br)c(C(F)(F)F)c1
Compound ( c )
CCOc1ccc(Br)c(C(F)(F)F)c1
2-bromo-5-ethoxybenzotrifluoride
CCCCCC.[Li][CH2]CCC
butyllithium hexane
Cl
hydrochloric acid
CC(C)OB(OC(C)C)OC(C)C
Triisopropyl borate
CCOc1ccc(OB(O)O)c(C(F)(F)F)c1
Compound ( d )
收率 89.1%
CCOc1ccc(OB(O)O)c(C(F)(F)F)c1
4-ethoxy-2-trifluoromethylphenylboric Acid
收率 89.1%

反应条件

温度
-78°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas then slowly added dropwise at −78° C.
  2. 2
    workup.STIRRINGthe mixture was stirred at the same temperature for 1 hour
  3. 3
    温度The temperature was increased to room temperature
  4. 4
    温度cooling temperature
  5. 5
    萃取the aqueous layer was extracted three times with ether
  6. 6
    洗涤washed with water
  7. 7
    干燥dried over anhydrous magnesium sulfate
  8. 8
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

实验过程

Compound (c) (10.0 g) dissolved in tetrahydrofuran (THF) (40 mL) was cooled to −78° C., a 1.6 M butyllithium/hexane solution (30 mL) was slowly added dropwise and the mixture was stirred at the same temperature for 2 hours. Triisopropyl borate (14.0 g) dissolved in THF (20 mL) was then slowly added dropwise at −78° C., and the mixture was stirred at the same temperature for 1 hour. The temperature was increased to room temperature and the final solution was stirred. After adding 3 M hydrochloric acid (200 mL) dropwise at ice-cooling temperature, the aqueous layer was extracted three times with ether. The organic layers were combined, washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 8.28 g of Compound (d).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07070838B2uspto-grants-2006_07