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Chemical Structure| 773135-56-1 Chemical Structure| 773135-56-1

Structure of 773135-56-1

Chemical Structure| 773135-56-1

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Product Details of [ 773135-56-1 ]

CAS No. :773135-56-1
Formula : C10H10F2O2
M.W : 200.18
SMILES Code : O=C(OCC)C1=CC=C(C)C(F)=C1F
MDL No. :MFCD06204526

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Application In Synthesis of [ 773135-56-1 ]

* 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 [ 773135-56-1 ]

[ 773135-56-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 261763-37-5 ]
  • [ 773135-56-1 ]
YieldReaction ConditionsOperation in experiment
95% With thionyl chloride; at 60℃; for 16.0h; To a solution of <strong>[261763-37-5]2,3-difluoro-4-methylbenzoic acid</strong> (17.43mmol, 3000 mg) in EtOH (20 ml) thionyl chloride (31 .4 mmol, 2.29 ml) was added. The mixture was stirred at 605C for 16h. Solvent was evaporated. It was washed twice with EtAcO/water. The combined organic layers were dried over Na2S04, filtered and evapotared. (3330 mg, yield: 95%). LC-MS: tR = 2.52 [M+H]+ = 201 (method 6)
91.3% With sulfuric acid;Reflux; In a 1L flask was placed <strong>[261763-37-5]2,3-difluoro-4-methylbenzoic acid</strong> (50.0 g, 290 mmol) and ethanol (300 mL). To the stirred mixture was added concentrated sulfuric acid (14.5 g, 0.5 eq). The reaction was heated to reflux and the temperature maintained overnight. The mixture was concentrated under reduced pressure at 40C and diluted with ethyl acetate (200 mL). The resulting solution was washed with water (100 mL), saturated NaHC03 solution (100 mL) and brine, dried over Na2S04, and concentrated under vacuum to give the title compound (53g, 91.3%) as a light yellow oil. LC/MS m/z = 201.2 [M+l]+.
 

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