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Chemical Structure| 1460306-41-5 Chemical Structure| 1460306-41-5

Structure of 1460306-41-5

Chemical Structure| 1460306-41-5

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Product Details of [ 1460306-41-5 ]

CAS No. :1460306-41-5
Formula : C15H14O4
M.W : 258.27
SMILES Code : COC(C1=CC(C2=C(C=CC(OC)=C2)O)=CC=C1)=O
MDL No. :MFCD27578711

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Application In Synthesis of [ 1460306-41-5 ]

* 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 [ 1460306-41-5 ]

[ 1460306-41-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 1215206-03-3 ]
  • [ 1460306-41-5 ]
YieldReaction ConditionsOperation in experiment
84% With thionyl chloride; for 2.0h;Reflux; Methyl 2'-hydroxy-5'-methoxybiphenyl-3-carboxylate (6) Thionyl chloride (5.14 mL, 71 mmol) was added at 0C to a soln of 5 (5.74 g, 23.5 mmol) in MeOH (100 mL). The mixture was heated to reflux for 2 h. Evaporation of the volatiles, aqueous workup (EtOAc, sat. aq. NaHCOs soln; Na2S04) and FC (hexane/EtOAc 4:1 ) afforded the ester 6 (5.1 g, 84%). Data of 6: Ci5Hi404 (258.3). H-NMR (DMSO-d6): 9.18 (s, OH); 8.17 (t, J = 1.7, 1 H); 7.89 (td, J = 1.4, 7.8, 1 H); 7.82 (td, J = 1.5, 8.0, 1 H); 7.56 (t, J = 7.8, 1 H); 6.91 - 6.78 (m, 3 H); 3.87 (s, 3 H); 3.72 (s, 3 H).
84% With thionyl chloride; for 2.0h;Reflux; Thionyl chloride (5.14 mE, 71 mmol) was added at0 C. to a soln of5 (5.74 g, 23.5 mmol) in MeOH (100 mE). The mixture was heated to reflux for 2 h. Evaporation of the volatiles, aqueous workup (EtOAc, sat. aq. NaHCO3 soln; Na2504) and FC (hexane/EtOAc 4:1) afforded the ester 6 (5.1 g, 84%).Data of 6: C15H1404 (258.3). ‘H-NMR (DMSOd 5): 9.18 (s, OH); 8.17 (t, J=1.7, 1H); 7.89 (td, J=1.4, 7.8, 1H); 7.82 (td, J=1.5, 8.0, 1H); 7.56 (t, J=7.8, 1H); 6.91-6.78 (m, 3H); 3.87 (s, 3H); 3.72 (s, 3H).
 

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