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Chemical Structure| 36809-08-2 Chemical Structure| 36809-08-2

Structure of 36809-08-2

Chemical Structure| 36809-08-2

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Product Details of [ 36809-08-2 ]

CAS No. :36809-08-2
Formula : C13H9ClO3
M.W : 248.66
SMILES Code : O=C(O)C1=CC=CC=C1OC2=CC=CC=C2Cl
English Name :2-(2-Chlorophenoxy)benzoic acid
MDL No. :MFCD06260646

Safety of [ 36809-08-2 ]

Application In Synthesis of [ 36809-08-2 ]

* 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 [ 36809-08-2 ]

[ 36809-08-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 149978-43-8 ]
  • [ 36809-08-2 ]
  • [ 3023681-73-1 ]
YieldReaction ConditionsOperation in experiment
With 1-methyl-1H-imidazole; N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate In dichloromethane at 20 - 40℃; 11 General procedure: At room temperature, into a 10 mL pressure-resistant tube, add 1 mmol of intermediate pyrazolamide II-a, 1.1mmol 2-phenoxybenzoic acid, 3mL anhydrous dichloromethane, 3.5mmol N-methylimidazole and 1.2mmol tetramethylchloroformamidinium hexafluorophosphate, then stir for 10 minutes, raise the temperature of the reaction system to 40°C and react for 4 hours. TLC traces the reaction. After the reaction is completed, after extraction, drying, concentration, and column passing, a yellow solid, compound I-1, was obtained with a yield of 51.5%;
With 1-methyl-1H-imidazole; N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate In dichloromethane at 20 - 40℃; 11 General procedure: At room temperature, into a 10 mL pressure-resistant tube, add 1 mmol of intermediate pyrazolamide II-a, 1.1mmol 2-phenoxybenzoic acid, 3mL anhydrous dichloromethane, 3.5mmol N-methylimidazole and 1.2mmol tetramethylchloroformamidinium hexafluorophosphate, then stir for 10 minutes, raise the temperature of the reaction system to 40°C and react for 4 hours. TLC traces the reaction. After the reaction is completed, after extraction, drying, concentration, and column passing, a yellow solid, compound I-1, was obtained with a yield of 51.5%;
With 1-methyl-1H-imidazole; N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate In dichloromethane
 

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