반응 #325536

ord-c46068df174a432ab0eb51e999a7ef4c

반응 방정식

Cn1nccc1B1OC(C)(C)C(C)(C)O1
1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
FC(F)(F)c1ccc(I)cc1
4-iodobenzotrifluoride
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCO
ethanol
Cn1nccc1-c1ccc(C(F)(F)F)cc1
title compound
수율 110.4%
Cn1nccc1-c1ccc(C(F)(F)F)cc1
1-Methyl-5-[4-(trifluoromethyl)phenyl]-1H-pyrazole
수율 110.4%

반응 조건

온도
75°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척was then washed with water
  2. 2
    건조The organic layer was dried over anhydrous magnesium sulfate
  3. 3
    농축was then concentrated under a reduced pressure
  4. 4
    기타The residue was purified by column chromatography (silica gel 60N, hexane:ethyl acetate=4:1 to 3:1)

실험 절차

Under a nitrogen atmosphere, a mixture of 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (4.00 g), 4-iodobenzotrifluoride (4.03 g), bis(triphenylphosphine)palladium(II) dichloride (312 mg), potassium carbonate (2.65 g), ethanol (10 mL) and dimethylformamide (20 mL) was stirred at 75° C. for 2 hours. Thereafter, the reaction solution was diluted with ethyl acetate, and was then washed with water. The organic layer was dried over anhydrous magnesium sulfate, and was then concentrated under a reduced pressure. The residue was purified by column chromatography (silica gel 60N, hexane:ethyl acetate=4:1 to 3:1), so as to obtain the title compound (3.70 g) in the form of a brownish-red solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08642626B2uspto-grants-2014_02