반응 #58823

ord-b41d6759d10b4b0cbed807edb4d0b8d3

반응 방정식

C#Cc1ccccc1
ethynylbenzene
FC(F)Oc1ccc(I)cc1
1-(difluoromethoxy)-4-iodobenzene
CN(C)C=O
N,N-dimethylformamide
CCN(CC)CC
triethylamine
FC(F)Oc1ccc(C#Cc2ccccc2)cc1
1-(difluoromethoxy)-4-(phenylethynyl)benzene
수율 76.4%

용매

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas introduced anhydrous argon for 5 minutes
  2. 2
    온도The mixture cooled to room temperature
  3. 3
    추출extracted with ethyl ether
  4. 4
    건조The organic extracts were dried over MgSO4
  5. 5
    기타Evaporation and purification on silica gel (ISCO)

실험 절차

Into a mixture of ethynylbenzene (1.9 g, 18.5 mmol), 1-(difluoromethoxy)-4-iodobenzene (5 g, 18.5 mmol), N,N-dimethylformamide (35 mL), and triethylamine (12.8 mL, 92.6 mmol) was introduced anhydrous argon for 5 minutes. Then, copper(I) iodide (1.85 mmol, 351 mg) and dichlorobis(triphenylphosphine)palladium(II) (1.11, 0.71 g) were added into the mixture and the new mixture was stirred at 60° C. for 3 hours. The mixture cooled to room temperature, poured into water and extracted with ethyl ether. The organic extracts were dried over MgSO4. Evaporation and purification on silica gel (ISCO) using hexanes/EtOAc (100/1) as the eluting solvent, gave 1-(difluoromethoxy)-4-(phenylethynyl)benzene as a clear oil (3.45 g, 76% yield). MS m/e M+ 244; 1H NMR (400 MHz, DMSO-d6) 7.2 (d, J=8.78 Hz, 2H), 7.28-7.45 (m, 4H), 7.5-7.55 (m, 2H), 7.6 (d, J=7.78 Hz, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07423158B2uspto-grants-2008_09