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Chemical Structure| 1049606-80-5 Chemical Structure| 1049606-80-5

Structure of 1049606-80-5

Chemical Structure| 1049606-80-5

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Product Details of [ 1049606-80-5 ]

CAS No. :1049606-80-5
Formula : C10H6ClNO2
M.W : 207.61
SMILES Code : O=C(C1=CC2=C(C(Cl)=N1)C=CC=C2)O
MDL No. :MFCD10686865

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Application In Synthesis of [ 1049606-80-5 ]

* 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 [ 1049606-80-5 ]

[ 1049606-80-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 349552-70-1 ]
  • [ 1049606-80-5 ]
YieldReaction ConditionsOperation in experiment
92% With sodium hydroxide; In ethanol; for 0.5h;Reflux; A mixture of 36 (133 mg, 0.6 mmol) in 1NNaOH : EtOH (1 : 1, 6 mL) was refluxed for 0.5 h. After cooled down, the reaction mixture wasconcentrated and adjusted to pH = 3 with 1N HCl. The resultant mixture was dried underreduced pressure. To the residue was added EtOH (20 mL) and refluxed for 5 min. Then it wassubjected to hot filtration. The collected solid was added EtOH (20 mL) and subjected to thesame procedure twice. The combined filtration was concentrated and crystallized withMeOH/Et2O to give 114 mg white solid, in 92% yield. 1H NMR (400 MHz, CD3OD) 8.62 (s,1H), 8.45 (m, 1H), 8.17 (m, 1H), 7.977.91 (m, 2H); 13C NMR (100 MHz, CD3OD) δ 167.21,152.65, 141.76, 138.93, 133.54, 132.39, 130.02, 129.45, 127.40, 125.35.
92% With sodium hydroxide; In ethanol; water; for 0.5h;Reflux; A mixture of 43 (133 mg, 0.6 mmol) in 1N NaOH: EtOH (1 : 1, 6 mL) was refluxed for 0.5 h. After cooled down, the reactionmixture was concentrated and adjusted to pH = 3 with 1N HCl. The resultantmixture was dried under reduced pressure. To the residue was added EtOH (20 mL)and refluxed for 5 min. Then it was subjected to hot filtration. The collectedsolid was added EtOH (20 mL) and subjected to the same procedure twice. Thecombined filtration was concentrated and crystallized with MeOH/Et2Oto give 114 mg white solid, in 92% yield. 1H NMR (400 MHz, CD3OD)d 8.62 (s, 1H), 8.45 (m, 1H), 8.17 (m, 1H), 7.97-7.91(m, 2H); 13C NMR (100 MHz, CD3OD) δ 167.21, 152.65, 141.76, 138.93, 133.54, 132.39, 130.02,129.45, 127.40, 125.35
 

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