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Chemical Structure| 850335-27-2 Chemical Structure| 850335-27-2

Structure of 850335-27-2

Chemical Structure| 850335-27-2

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Product Details of [ 850335-27-2 ]

CAS No. :850335-27-2
Formula : C8H6FNO5
M.W : 215.14
SMILES Code : O=C(OC)C1=CC([N+]([O-])=O)=C(O)C(F)=C1
MDL No. :MFCD16038819

Safety of [ 850335-27-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H315-H317-H318-H410
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 850335-27-2 ]

* 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 [ 850335-27-2 ]

[ 850335-27-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 403-01-0 ]
  • [ 850335-27-2 ]
YieldReaction ConditionsOperation in experiment
100% With methyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carboxylate; In diethyl ether; water; at -10 - 20℃; for 16h; 65% aq. nitric acid solution (2.3 mL, 50 mmol) and fuming nitric acid (2.1 mL, 50 mmol) were added at -10 C. to a solution of 4-hydroxy-3-trifluoromethyl-benzoic acid methyl ester (4.27 g, 25.1 mmol) in diethyl ether (60 mL). The ice bath was removed and the reaction mixture was stirred at room temperature for 16 h, then partitioned between water and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to afford 3-fluoro-4-hydroxy-5-nitro-benzoic acid methyl ester (5.39 g, 100%). Yellow solid, MS (ISP)=214.1 (M-H)-.
80% With nitric acid; In diethyl ether; at -10 - 27℃; for 2h; Into a 500-mL 3-necked round-bottom flask, was placed methyl 3-fluoro-4- hydroxybenzoate (4.27 g, 25.10 mmol, 1.00 equiv), ether (200 mL). This was followed by the addition of nitric acid (65%) (3.48 mL, 50.24 mmol, 2.00 equiv) dropwise with stirring at -10 C. To this was added fuming nitric acid (2.15 mL, 50.23 mmol, 2.00 equiv) dropwise with stirring at -10 C. The resulting solution was stirred for 2 h at room temperature (27 C) and then slowly poured into 100 mL of water/ice. The mixture was extracted with 2x100 mL of dichlorom ethane, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified via column chromatography on silica gel (eluting with ethyl acetate/petroleum ether (1 : 1)) to afford methyl 3-fluoro-4-hydroxy-5-nitrobenzoate (4.3 g, 80% as a yellow solid. MS: (ESI, m/z): 214[M-H]".
 

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