反応 #6687

ord-3e1233a3cb904efd828fd79e64ba9c58

反応方程式

CC(C)OB(OC(C)C)OC(C)C
triisopropylborate
CCCCCOCCCCOc1cccc(F)c1F
1,2-difluoro-3-(4-pentyloxybutoxy)-benzene
CCCCCOCCCCOc1cccc(F)c1F
1,2-Difluoro-3-(4-pentyloxybutoxy)benzene
[Li][CH2]CCC
butyllithium
CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
2,3-Difluoro-4-(4-pentyloxybutoxy)phenylboronic acid

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at that temperature for 1 h and at room temperature for 10 h
  2. 2
    その他quenched with water
  3. 3
    抽出extracted with ethyl acetate
  4. 4
    洗浄washed with brine
  5. 5
    乾燥dried over MgSO4
  6. 6
    濃縮concentrated in vacuo
  7. 7
    その他Purification
  8. 8
    その他by recrystallization from hexane

実験手順

To a solution of 1,2-difluoro-3-(4-pentyloxybutoxy)-benzene (24), (1 equi.) in THF (5 mL/mmole), butyllithium (1.3 equi.) was added at −78° C. The reaction mixture was stirred at that temperature for 2 h,. Then triisopropylborate (1 equi.) was added at that temperature. The reaction mixture was stirred at that temperature for 1 h and at room temperature for 10 h, quenched with water, extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by recrystallization from hexane gave 2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid (25), as a white solid (75%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07083832B2uspto-grants-2006_08