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Chemical Structure| 116355-65-8 Chemical Structure| 116355-65-8

Structure of 116355-65-8

Chemical Structure| 116355-65-8

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Product Details of [ 116355-65-8 ]

CAS No. :116355-65-8
Formula : C9H8FNO5
M.W : 229.16
SMILES Code : O=C(OC)COC1=CC(F)=CC=C1[N+]([O-])=O
MDL No. :MFCD00117826

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Application In Synthesis of [ 116355-65-8 ]

* 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 [ 116355-65-8 ]

[ 116355-65-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 116355-65-8 ]
  • [ 103361-99-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;palladium-carbon; In ethanol; b. 7-fluoro-2H-1,4-benzoxazin-3(4H)-one To 500 mg of 5% Pd/C in a Parr bottle was added 100 ml of EtOH followed by 5.0 g (21.8 mmol) of methyl 5-fluoro-2-nitrophenoxyacetate. The flask was placed in a Parr Apparatus, evacuated and then charged with hydrogen. The suspension was then shaken for 2 hours. After evacuating the flask and recharging with nitrogen, the solids were removed by vacuum filtration through Celite. Since some product does precipitate, the filter cake is repeatedly rinsed with EtOAc (200 ml). The filtrate is refluxed for 4 hours and then evaporated to dryness in vacuo to give the desired material, 7-fluoro-2H-1,4-benzoxazin-3(4H)-one, as a white solid (m.p. 201-202 C.) in quantitative yield.
With hydrogen;palladium-carbon; In ethanol; b. 7-fluoro-2H-1,4-benzoxazin-3(4H)-one To 500 mg of 5% Pd/C in a Parr bottle was added 100 ml of EtOH followed by 5.0 g (21.8 mmol) of methyl 5-fluoro-2-nitrophenoxyacetate. The flask was placed in a Parr Apparatus, evacuated and then charged with hydrogen. The suspension was then shaken for 2 hours. After evacuating the flask and recharging with nitrogen, the solids were removed by vacuum filtration through Celite. Since some product does precipitate, the filter cake is repeatedly rinsed with EtOAc (200 ml). The filtrate is refluxed for 4 hours and then evaporated to dryness in vacuo to give the desired material, 7-fluoro-2H-1,4-benzoxazin-3(4H)-one, as a white solid (m.p. 201-202 C.) in quantitative yield.
 

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