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Chemical Structure| 533897-93-7 Chemical Structure| 533897-93-7

Structure of 533897-93-7

Chemical Structure| 533897-93-7

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Product Details of [ 533897-93-7 ]

CAS No. :533897-93-7
Formula : C15H13NO5
M.W : 287.27
SMILES Code : O=C(C1=CC=CC(OCC2=CC=CC=C2)=C1[N+]([O-])=O)OC
MDL No. :MFCD27976472

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Application In Synthesis of [ 533897-93-7 ]

* 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 [ 533897-93-7 ]

[ 533897-93-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 89942-77-8 ]
  • [ 100-44-7 ]
  • [ 533897-93-7 ]
  • 2
  • [ 89942-77-8 ]
  • [ 100-39-0 ]
  • [ 533897-93-7 ]
YieldReaction ConditionsOperation in experiment
91% With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 100℃; for 2h; A mixture of part A compound (1.0 g, 5.07 mmol) and potassium carbonate (700 mg, 5.07 mmol) in dry DMF (10 mL) was treated with benzyl bromide (992 mg, 5.8 mmol) and heated at 100 C. for 2 h. The mixture was concentrated and partitioned between EtOAc (3×50 mL) and water (10 mL). The organic phase was washed with H2O ( 3×10 mL) and brine (10 mL), dried (MgSO4) and evaporated. Purification by flash chromatography (2.5×25 cm column, 1:4 EtOAc/hexane) provided the title compound as a white solid (1.32 g, 91% yield), mp 96-98 C.
89% A solution of <strong>[89942-77-8]methyl <strong>[89942-77-8]3-hydroxy-2-nitrobenzoate</strong></strong> (6.9 g, 0.033 mol) in dry DMF (100 ml) was cooled to 0 C under argon and treated with sodium hydride (0.96 g, 0.04 mol). The reaction mixture was stirred for 10 min and benzyl bromide (6.27 g, 0.036 mol) was added. The reaction mixture was allowed to warm to 25 C, and stirring was continued for an additional 20 h. A solution of saturated NaCl (30 ml) was added, and the reaction mixture was further diluted with H2O (100 ml). The aqueous layer was extracted with Et2O (4 150 ml). The combined ether extracts were washed with H2O (100 ml), washed with saturated NaCl (30 ml), dried over Na2SO4 and the solvent was removed in vacuum. Then CHCl3 was added (30 ml), and the solution was dried over Na2SO4 and evaporated in vacuum to yield methyl 3-(benzyloxy)-2-nitrobenzoate as yellow crystals (89% yield, 8.95 g). 1H NMR delta = 7.58 (dd, 1H, aromaticH), 7.23-7.45 (m, 7H, phenyl and aromatic Hs), 5.19 (s, 2H,PhCH2), 3.88 (CO2CH3, s, 3H).
 

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