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Chemical Structure| 217978-01-3 Chemical Structure| 217978-01-3

Structure of 217978-01-3

Chemical Structure| 217978-01-3

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Product Details of [ 217978-01-3 ]

CAS No. :217978-01-3
Formula : C9H9FO3
M.W : 184.16
SMILES Code : O=C(OCC)C1=CC=C(O)C=C1F
MDL No. :MFCD12025352

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Application In Synthesis of [ 217978-01-3 ]

* 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 [ 217978-01-3 ]

[ 217978-01-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38222-83-2 ]
  • [ 217978-01-3 ]
  • [ 345963-90-8 ]
YieldReaction ConditionsOperation in experiment
85% With trifluoromethanesulfonic acid anhydride; In hexane; dichloromethane; Ethyl-2-fluoro-4-trifluoromethylsulfonyloxy-benzoate (Intermediate 6) A stirred, cooled (ice bath) solution of ethyl-2-fluoro-4-hydroxy-benzoate (Intermediate 5, 0.368 g, 2 mmol) and 2,6-di-tert-butyl-4-methyl-pyridine (0.81 g, 8 mmol) in 8 mL of dichloromethane was treated with trifluoromethanesulfonic anhydride (0.1 g, 4 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was subjected to flash column chromatography over silica gel (230-400 mesh) using 5-10percent ethyl acetate in hexane as the eluent to afford the title compound (0.53 g, 85percent). 1H-NMR (300 MHz, CDCl3): delta1.41 (t, J=7.3 Hz, 3H), 4.42 (q, J=7.1 Hz, 2H), 7.12-7.20(m, 2H), 8.08(t, J=8.3 Hz, 1H).
85% With trifluoromethanesulfonic acid anhydride; In hexane; dichloromethane; Ethyl-2-fluoro-4-trifluoromethylsulfonyloxy-benzoate (Intermediate 6) A stirred, cooled (ice bath) solution of ethyl-2-fluoro-4-hydroxy-benzoate (Intermediate 5, 0.368 g, 2 mmol) and 2,6-di-tertbutyl-4-methyl-pyridine (0.81 g, 8 mmol) in 8 mL of dichloromethane was treated with trifluoromethanesulfonic anhydride (0.1 g, 4 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was subjected to flash column chromatography over silica gel (230-400 mesh) using 5-10percent ethyl acetate in hexane as the eluent to afford the title compound (0.53 g, 85percent). 1H-NMR (300 MHz, CDCl3): delta 1.41 (t, J=7.3 Hz, 3H), 4.42 (q, J=7.1 Hz, 2H), 7.12-7.20(m, 2H), 8.08(t, J=8.3 Hz, 1H).
 

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