Reacción #6687

ord-3e1233a3cb904efd828fd79e64ba9c58

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at that temperature for 1 h and at room temperature for 10 h
  2. 2
    Otroquenched with water
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    Lavadowashed with brine
  5. 5
    Secadodried over MgSO4
  6. 6
    Concentraciónconcentrated in vacuo
  7. 7
    OtroPurification
  8. 8
    Otroby recrystallization from hexane

Procedimiento

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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07083832B2uspto-grants-2006_08