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Chemical Structure| 2585-26-4 Chemical Structure| 2585-26-4

Structure of 2585-26-4

Chemical Structure| 2585-26-4

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Product Details of [ 2585-26-4 ]

CAS No. :2585-26-4
Formula : C14H12N2O3
M.W : 256.26
SMILES Code : O=C(NCC1=CC=CC=C1)C2=CC=C([N+]([O-])=O)C=C2
MDL No. :MFCD00431000

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Application In Synthesis of [ 2585-26-4 ]

* 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 [ 2585-26-4 ]

[ 2585-26-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2585-26-4 ]
  • [ 54977-92-3 ]
YieldReaction ConditionsOperation in experiment
91% General procedure: The aromatic nitro compounds are dissolved in ethyl acetate and SnCl2 × 2H2O (1.125 g/mmol) is added. The reaction mixture is heated under reflux for at least 2 h. The reaction is monitored by thin layer chromatography. When the reaction is completed, the batch is cooled. A solution of NaHCO3 is then added until pH 7-8 is reached. The organic layer is separated and the aqueous residue is washed three times with ethyl acetate. The combined organic layers are washed with brine and dried over MgSO4. The solvent is removed in vacuo to obtain the crude product.
85% With hydrogenchloride; tin; In ethanol; water;Reflux; General procedure: Concentrated HCl (10-15 ml) was added slowly to a mixture of 4-nitrobenzenesulfonamide or 4-nitrobenzamide analog (13a-q,1.4 mmol, 1 eq) and Sn granules (2-2.5 eq) in ethanol (10 mL). The reaction mixture was refluxed for 3.5-6 h. When the TLC plates howed that there is no more starting material left, the reaction mixture was cooled down to rt. NaOH (30% or 5M, aq) was added to the mixture until it became basic. The mixture was extracted with EA or DCM and the organic layer was dried with Na2SO4. The solvent was evaporated. The product was purified with column chromatography when required. 4.6.4.23 4-Amino-N-benzylbenzamide (14f) From 13f (0.89 g, 3.5 mmol) with general procedure B. Light yellow solid (0.67 g, 85%). 1H NMR (DMSO-d6): δ 4.42 (2H, d, J = 6.0 Hz), 5.60 (2H, s), 6.54 (2H, d, J = 8.6 Hz), 7.21 (1H, m), 7.29 (4H, m), 7.61 (2H, d, J = 8.6 Hz), 8.54 (1H, t, J = 5.9 Hz).
 

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