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Chemical Structure| 773134-94-4 Chemical Structure| 773134-94-4

Structure of 773134-94-4

Chemical Structure| 773134-94-4

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Product Details of [ 773134-94-4 ]

CAS No. :773134-94-4
Formula : C10H8F4O2
M.W : 236.16
SMILES Code : O=C(OCC)C1=CC(C(F)(F)F)=CC=C1F
MDL No. :MFCD06204412

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Application In Synthesis of [ 773134-94-4 ]

* 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 [ 773134-94-4 ]

[ 773134-94-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 207981-46-2 ]
  • [ 64-17-5 ]
  • [ 773134-94-4 ]
YieldReaction ConditionsOperation in experiment
92% With triethylamine; In tetrahydrofuran; at 20℃; for 1h; Example 146; N-r(5Z)-2-tert-butyl-4-isobutylisothiazol-5(2H)-ylidene]-2-ethoxy-5- (trifluoromethyl)benzamide; Example 146 A; ethyl 2-fluoro-5-(trifluoromethyl)benzoate; To a solution of <strong>[207981-46-2]2-fluoro-5-(trifluoromethyl)benzoyl chloride</strong> (5.0 g, 22.0 mmol) in THF (25 mL) was added Et3N (3.1 mL, 22.0 mmol) followed by EtOH (1.3 mL, 22.0 mmol). This mixture was stirred at ambient temperature for 1 h and quenched with saturated, aqueous NH4Cl (10 mL). The layers were separated and the aqueous layer was extracted with 3 X 10 mL EtOAc and the combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography (SiO2, 60% hexanes in EtOAc) to give the title compound (4.8 g, 20.3 mmol, 92% yield). 1H NMR (300 MHz, CDCl3) δ ppm 1.42 (t, J=7.1 Hz, 3 H), 4.43 (q, J=7.1 Hz, 2 H), 7.23 - 7.34 (m, 1 H), 7.74 - 7.82 (m, 1 H), 8.23 (dd, J=6.3, 2.4 Hz, 1 H).
92% With triethylamine; In tetrahydrofuran; at 20℃; for 1h; Example 146 A; ethyl 2-fluoro-5 -(trifluoromethyl)benzoate; To a solution of <strong>[207981-46-2]2-fluoro-5-(trifluoromethyl)benzoyl chloride</strong> (5.0 g, 22.0 mmol) in THF (25 mL) was added Et3N (3.1 mL, 22.0 mmol) followed by EtOH (1.3 mL, 22.0 mmol). This mixture was stirred at ambient temperature for 1 h and quenched with saturated, aqueous NH4Cl (10 mL). The layers were separated and the aqueous layer was extracted with 3 X 10 mL EtOAc and the combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography (SiO2, 60% hexanes in EtOAc) to give the title compound (4.8 g, 20.3 mmol, 92% yield). 1H NMR (300 MHz, CDCl3) δ ppm 1.42 (t, J=I λ Hz, 3 H), 4.43 (q, J=7.1 Hz, 2 H), 7.23 - 7.34 (m, 1 H), 7.74 - 7.82 (m, 1 H), 8.23 (dd, J=6.3, 2.4 Hz, 1 H).
 

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