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Chemical Structure| 957146-67-7 Chemical Structure| 957146-67-7

Structure of 957146-67-7

Chemical Structure| 957146-67-7

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Product Details of [ 957146-67-7 ]

CAS No. :957146-67-7
Formula : C8H4F6O
M.W : 230.11
SMILES Code : FC(C1=CC=C(F)C(OC(F)F)=C1)(F)F
MDL No. :MFCD11847322

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Application In Synthesis of [ 957146-67-7 ]

* 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 [ 957146-67-7 ]

[ 957146-67-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1895-39-2 ]
  • [ 141483-15-0 ]
  • [ 957146-67-7 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In water; N,N-dimethyl-formamide; at 100℃; for 2h;Product distribution / selectivity; To a stirred solution of <strong>[141483-15-0]2-fluoro-5-trifluoromethyl-1-phenol</strong> (9.9 g, 54.9 mmol) in 100 ml of DMF (100 mL) and water (10 mL) was added sodium chlorodifluoroacetate (20.9 g, 137.2 mmol) and cesium carbonate (26.8 g, 82.3 mmol). The reaction mixture was stirred at 100 C. for 2 hours. After it cooled to room temperature, it was diluted with ethyl acetate (700 ml), washed with water (3×) and brine, dried over magnesium sulfate, filtered and concentrated. The crude product (colorless oil, volatile) was used for the next step without further treatment. 1H NMR (CDCl3, delta ppm): 6.6 (t, 1H), 7.3 (m, 1H), 7.6 (m, 2H).
With potassium carbonate; In N,N-dimethyl-formamide; at 19 - 97℃; for 2h;Product distribution / selectivity; A 100-L round bottom flask equipped with overhead stirrer, thermocouple, nitrogen inlet, condenser and steam bath was charged with <strong>[141483-15-0]2-fluoro-5-(trifluoromethyl)phenol</strong> (5.50 kg), sodium chlorodifluoroacetate (9.31 kg), and DMF (4 L). There was an exotherm to 46.7 C. when the 4 L of DMF was charged to the flask. The temperature of the reaction was immediately reduced to 19 C. by rapid cooling with an ice/water bath. An additional 37.3 L of DMF (total DMF, 41.3 L) was then slowly charged, maintaining the internal temperature below 30 C. After cooling to ambient temperature, water (5.5 L) was charged, resulting in a 10 C. exotherm. Potassium carbonate (5.28 kg) was then added. The ice water bath was removed and the batch was heated to 97 C. using a steam bath. The reaction was complete after aging for 2 h at 97 C., as evidenced by HPLC assay, with <1% starting material remaining. The reaction was cooled to ambient temperature, and water (42 L) was slowly added. The batch was transferred to a 170-L extractor and extracted with MTBE (2×18 L). The organic layers were combined and washed with water (1×11 L) and brine (1×11 L). The MTBE solution was pumped into a 22-L flask equipped with a thermocouple, distillation apparatus, and a heating mantle. The MTBE was distilled off at 55-118 C. and atmospheric pressure. The desired product was purified by distillation at 120-157 C. and atmospheric pressure, and was isolated as a clear oil.
With caesium carbonate; In water; N,N-dimethyl-formamide; at 100℃; for 3h; Sodium chlorodifluoroacetate (1.091 g, 6.94 mmol) and cesium carbonate (1.357 g, 4.16 mmol) were added to an N, N-dimethylformarmde (5 mL) solution of 2-fluoro-5-trifluoromethyl phenol containing 10 volume % water (0.55 mL), and the reaction mixture was heated for 3 h at 1000C. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate and washed with water (3 X), brine (1 X) The organic layer was d?ed over sodium sulfate and concentrated to obtain the desired product (650 mg), which was used in the next step without further purification.
 

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