Reaktion #6693

ord-88ca5467e26b4c35bf2cc8686a6850bf

Reaktionsgleichung

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-Difluoro4-(4-pentyloxybutoxy)phenylboronic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at that temperature for 1 h and at room temperature for 10 h
  2. 2
    Sonstigequenched with water
  3. 3
    Extraktionextracted with ethyl acetate
  4. 4
    Waschenwashed with brine
  5. 5
    Trocknendried over MgSO4
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    SonstigePurification
  8. 8
    Sonstigeby recrystallization from hexane

Vorschrift

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 hr,. 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%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07083832B2uspto-grants-2006_08