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Chemical Structure| 66411-31-2 Chemical Structure| 66411-31-2

Structure of 66411-31-2

Chemical Structure| 66411-31-2

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Product Details of [ 66411-31-2 ]

CAS No. :66411-31-2
Formula : C9H7NO6
M.W : 225.16
SMILES Code : O=C(C1=C2OCCOC2=CC=C1[N+]([O-])=O)O
MDL No. :MFCD22056322

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Application In Synthesis of [ 66411-31-2 ]

* 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 [ 66411-31-2 ]

[ 66411-31-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4442-53-9 ]
  • [ 66411-31-2 ]
YieldReaction ConditionsOperation in experiment
69% With nitric acid; acetic anhydride; acetic acid; at 40 - 45℃; for 2h; A solution of 2,3-dihydrobenzo [b] [1,4] dioxin-5-carboxylic acid (1 g, 5.56 mmol)Soluble in 4mL glacial acetic acid and 4mL acetic anhydride,After heating to 40 ° C,To this was added 0.6 mL of nitric acid and 0.6 mL of glacial acetic acid,Maintain the temperature 40 -45 heating two hours after the end of the reaction,Cool to room temperature.Add water to filter,The filtrate is placed in a refrigerator to cool the crystalline solid to precipitate,Get yellow crystal. Yield: 69percent.
With nitric acid; acetic anhydride; acetic acid; at 40 - 45℃; for 2h; A solution of 2,3-dihydrobenzo[b][1,4]dioxine-5-carbonylic acid (1 g, 5.56 mmol) in 4 ml of acetic acid and 4 ml of acetic anhydride was heated to 40°C, and a solution 0.6 ml nitric acid in 0.6 ml acetic acid was added. The mixture was stirred at 40-45°C for 2h and then cooled to 5°C. The precipitate was filtered with suction filter, washed with 10 ml water, collected and dried to afford 700 mg of the title compound as white solid, which was used in the next stepwithout further purification. LCMS (ESI) calc?d for C9H7N06, [M+H]: 226, found: 226.
 

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