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Chemical Structure| 149506-24-1 Chemical Structure| 149506-24-1

Structure of 149506-24-1

Chemical Structure| 149506-24-1

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Product Details of [ 149506-24-1 ]

CAS No. :149506-24-1
Formula : C14H11NO4
M.W : 257.24
SMILES Code : O=C(C1=CC(C2=CC=CC([N+]([O-])=O)=C2)=CC=C1)OC
MDL No. :MFCD06803017

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Application In Synthesis of [ 149506-24-1 ]

* 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 [ 149506-24-1 ]

[ 149506-24-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 618-89-3 ]
  • [ 13331-27-6 ]
  • [ 149506-24-1 ]
YieldReaction ConditionsOperation in experiment
26% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In water; toluene; at 20 - 80℃; for 5h;Inert atmosphere; [000408] Synthesis of methyl 3’-nitro-[l, 1’-biphenylj-3-carboxylate (515): To a stirred solution of <strong>[618-89-3]methyl 3-bromobenzoate</strong> 514 (2.5 g, 14.99 mmol) and (3-nitrophenyl) boronic acid 382 (3.8 g, 17.99 mmol) in toluene (20 mL) under inert atmosphere were added sodium carbonate (3.17 g, 29.99 mmol in 20 mL of H20) at RT and purged under argon atmosphere for 20 mm. To this was added Pd(PPh3)4 (693 mg, 0.59 mmol) and heated to 80 C for 5 h. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was diluted with EtOAc (200 mL). The organic extract was dried over sodium sulfate, filtered and concentrated in vacuo to obtain the crude. The crude was purified through silica gel column chromatography using 10% EtOAc/ hexanes to afford compound 515 (1 g, 26%) as yellow liquid. TLC: 15% EtOAc/ hexanes (R 0.5); 1H NMR (400 MHz, DMSO-d6): ö 8.48-8.46 (m, 1H), 8.30-8.25 (m, 2H), 8.22-8.18 (m, 1H), 8.11-8.07 (m, 1H), 8.04 (dt,J 7.8, 1.3 Hz, 1H),7.80 (t, J= 8.0 Hz, 1H), 7.69 (t, J= 7.8 Hz, 1H), 3.91 (s, 3H).
With palladium 10% on activated carbon; sodium carbonate; In methanol;Reflux; [0089] A mixture of (3-nitrophenyl)boronic acid and <strong>[618-89-3]methyl 3-bromobenzoate</strong> was placed into a reaction vessel with 10% palladium on carbon (Pd/C) and sodium carbonate (Na2C03) in methanol (MeOH). The reaction mixture was held at reflux until the starting materials had been converted into methyl 3'-nitro-[l1,1]-biphenyl]-3-carboxylate. The methyl 3'-nitro-[1,1]biphenyl]-3-carboxylate was maintained in the reaction vessel, used without purification, isopropyl acetate was added to the reaction vessel and the mixture subsequently reacted with 10% Pd/C in a hydrogen atmosphere to yield methyl 3'-amino-[1,1]-biphenyl]- 3-carboxylate.
 

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