反应 #2139925

ord-e0f9b6fa3e8a4ccfb56e33a6f98ebe39

反应方程式

Cl
HCl
[Li][CH2]CCC
butyllithium
Brc1ccccc1-c1ccccc1
bromobiphenyl
COB(OC)OC
trimethylborate
OB(O)c1ccc(-c2ccccc2)cc1
biphenylboronic acid

反应条件

温度
-95°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGat −95° C., and the solution was stirred for 2 hours at −78° C.
  2. 2
    workup.WAITfor 12 hours at room temperature
  3. 3
    其他at 0° C.
  4. 4
    workup.DISTILLATIONthe solvent was distilled
  5. 5
    萃取The reaction product was extracted with ether

实验过程

5 g of bromobiphenyl was dissolved in 100 mL of tetrahydrofuran(THF), and the solution was cooled to −95° C. Then, 20.2 mL of 1.6M butyllithium was added thereto and stirred for 5 minutes. 24.31 mL of trimethylborate was added thereto at −95° C., and the solution was stirred for 2 hours at −78° C., and for 12 hours at room temperature. Then, 10% HCl solution was added thereto at 0° C. to adjust the pH of the solution to be less than 6, and the solvent was distilled. The reaction product was extracted with ether to obtain biphenylboronic acid. Thereafter, as shown in the following reaction 4, 0.08 g of bromospiro-dimer, 0.034 g of biphenyl boric acid, 0.003 g of Pd(TPP)4 catalyst, 0.11 ml of 2M Na2CO3 were refluxed in 1,2-dimethoxyethane solvent while stirring for 24 hours (Suzuki coupling reaction) to obtain the target compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07326474B2uspto-grants-2008_02