반응 #624613

ord-3ecda96f054e4f1eaa68ba74b6eae076

반응 방정식

[Cl-].[NH4+]
ammonium chloride
N#Cc1ccc(F)cc1
4-fluorobenzonitrile
FC(F)(F)c1cn[nH]c1
4-(trifluoromethyl)-1H-pyrazole
[H-].[Na+]
sodium hydride
N#Cc1ccc(-n2cc(C(F)(F)F)cn2)cc1
4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)benzonitrile
수율 72.3%

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the reaction was heated to 80° C. overnight
  2. 2
    추출the mixture extracted with ethyl acetate
  3. 3
    건조The organic layer was dried over sodium sulfate
  4. 4
    여과filtered
  5. 5
    농축concentrated
  6. 6
    기타Purification by column chromatography

실험 절차

To a 0° C. solution of 4-(trifluoromethyl)-1H-pyrazole (1 g, 7 mmol) in N,N-dimethylformamide (10 mL) was added 60 wt % sodium hydride (132 mg, 3.31 mmol). The mixture was stirred at 0° C. for 30 minutes, 4-fluorobenzonitrile (979 mg, 8.08 mmol) was added and the reaction was heated to 80° C. overnight. Saturated ammonium chloride was added and the mixture extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated. Purification by column chromatography gave 4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)benzonitrile (1.2 g, 72%). 1H NMR (400 MHz, CD3OD, δ): 8.84 (s, 1H), 7.96 (s, 1H), 7.95 (d, 2H), 7.78 (d, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08859591B2uspto-grants-2014_10