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Chemical Structure| 881673-53-6 Chemical Structure| 881673-53-6

Structure of 881673-53-6

Chemical Structure| 881673-53-6

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Product Details of [ 881673-53-6 ]

CAS No. :881673-53-6
Formula : C14H12F3NO3
M.W : 299.25
SMILES Code : FC(F)(F)C1=C(C=CC=C1)C(CC(C(OCC)=O)C#N)=O
MDL No. :MFCD31543864

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Application In Synthesis of [ 881673-53-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 881673-53-6 ]

[ 881673-53-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 54109-16-9 ]
  • [ 881673-53-6 ]
YieldReaction ConditionsOperation in experiment
Reference Example 5 ethyl 2-cyano-4-oxo-4-[(2-trifluoromethyl)phenyl]butanoate; 2'-(Trifluoromethyl)acetophenone (10.0 g) was dissolved in chloroform (30 mL) and diethyl ether (30 mL), a solution of bromine (8.50 g) in chloroform (20 mL) was added dropwise while maintaining the reaction temperature at not higher than 25 C. After the dropwise addition, the mixture was stirred at room temperature for 1 hr, water was added to the reaction mixture and the mixture was extracted with chloroform. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, concentration under reduced pressure to give crude 2-bromo-1-(2-trifluoromethylphenyl)ethanone. Potassium carbonate (13.82 g) was added to ethyl cyanoacetate (44.44 g), and the mixture was stirred at 45 C. for 1 hr. A solution of crude 2-bromo-1-(2-trifluoromethylphenyl)ethanone in acetone (100 mL) was added dropwise. After completion of the dropwise addition, the mixture was stirred at the same temperature for 1 hr, and stirred overnight at room temperature. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Excess ethyl cyanoacetate contained in the obtained oil was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→7:1) to give the title compound as an oil (yield 10.43 g, from 2'-(trifluoromethyl)acetophenone, yield 66%). 1H-NMR (CDCl3) δ: 1.36 (3H, t, J=7.2 Hz), 3.34-3.46 (1H, m), 3.59-3.70 (1H, m), 4.08-4.22 (1H, m), 4.32 (2H, q, J=7.2 Hz), 7.57-7.80 (4H, m).
  • 2
  • [ 54109-16-9 ]
  • [ 105-56-6 ]
  • [ 881673-53-6 ]
YieldReaction ConditionsOperation in experiment
10.43 g Potassium carbonate (13.82 g) was added to ethyl cyanoacetate (44.44 g), and the mixture was stirred at 45C for 1 hr. A solution (100 mL) of crude 1-bromo-1-(2-trifluoromethylphenyl)ethanone in acetone was added dropwise. After completion of the dropwise addition, the mixture was stirred at the same temperature for 1 hr, and stirred overnight at room temperature. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Excess ethyl cyanoacetate contained in the obtained oil was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→7:1) to give the title compound as an oil (yield 10.43 g, from 2'-(trifluoromethyl)acetophenone, 66%).1H-NMR (CDCl3)δ: 1.36 (3H, t, J=7.2 Hz), 3.34-3.46 (1H, m), 3.59-3.70 (1H, m), 4.08-4.22 (1H, m), 4.32 (2H, q, J=7.2 Hz), 7.57-7.80 (4H, m).
General procedure: K2CO3 powder (27.6 g, 200 mmol) was added to ethyl cyanoacetate (79.2 g 700 mmol), and the mixture was stirred at 43-45 C for 45 min. To this stirred suspension was added a solution of crude 2-bromo-1-(2-methylphenyl)ethanone in acetone (150 mL) over a period of 30 min, and then the mixture was stirred at room temperature for 16 h, filtered and concentrated under reduced pressure. The residue was taken up with EtOAc, washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting residue was purified by silica gel column chromatography (n-hexane/EtOAc = 10/1-8/1)to
 

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