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Chemical Structure| 6972-47-0 Chemical Structure| 6972-47-0

Structure of 6972-47-0

Chemical Structure| 6972-47-0

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Product Details of [ 6972-47-0 ]

CAS No. :6972-47-0
Formula : C8H7Cl3O
M.W : 225.50
SMILES Code : OC1=C(Cl)C(C)=C(Cl)C(C)=C1Cl
English Name :2,4,6-trichloro-3,5-dimethylphenol
MDL No. :MFCD00019986

Safety of [ 6972-47-0 ]

Application In Synthesis of [ 6972-47-0 ]

* 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 [ 6972-47-0 ]

[ 6972-47-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 133-53-9 ]
  • [ 6972-47-0 ]
YieldReaction ConditionsOperation in experiment
With chlorine
  • 2
  • [ 108-68-9 ]
  • [ 19523-54-7 ]
  • [ 527-61-7 ]
  • [ 133-53-9 ]
  • [ 6972-47-0 ]
YieldReaction ConditionsOperation in experiment
1: 52 % 2: 24 % 3: 15 % 4: 6 % With chlorine dioxide In dichloromethane; N,N-dimethyl-formamide at 6℃; Oxidation of phenols with ClO2. Method B. General procedure: Dimethylformamide (1 or 2 mL, depending on the amount of ClO2 used) was added to a mixture of the starting phenol (2 mmol) and a solution of ClO2 in CH2Cl2 (the molar ratio of phenol : ClO2 = 1 : 1 or 1 : 2). The reaction mixture was stirred for 1 h at room temperature or at 6 °C. After the reaction completion, the mixture was washed with water acidified with HCl. The organic layer was dried with anhydrous Na2SO4. The solvent was evaporated under reduced pressure. The reaction products were separated by column chromatography, using chloroform as an eluent.
1: 52 % 2: 24 % 3: 15 % 4: 6 % With chlorine dioxide In dichloromethane; N,N-dimethyl-formamide at 6℃; Oxidation of phenols with ClO2. Method B. General procedure: Dimethylformamide (1 or 2 mL, depending on the amount of ClO2 used) was added to a mixture of the starting phenol (2 mmol) and a solution of ClO2 in CH2Cl2 (the molar ratio of phenol : ClO2 = 1 : 1 or 1 : 2). The reaction mixture was stirred for 1 h at room temperature or at 6 °C. After the reaction completion, the mixture was washed with water acidified with HCl. The organic layer was dried with anhydrous Na2SO4. The solvent was evaporated under reduced pressure. The reaction products were separated by column chromatography, using chloroform as an eluent.
1: 44 % 2: 29 % 3: 21 % 4: 6 % With chlorine dioxide In DMF-d6 at 6℃; Oxidation of phenols with ClO2. Method B. General procedure: Dimethylformamide (1 or 2 mL, depending on the amount of ClO2 used) was added to a mixture of the starting phenol (2 mmol) and a solution of ClO2 in CH2Cl2 (the molar ratio of phenol : ClO2 = 1 : 1 or 1 : 2). The reaction mixture was stirred for 1 h at room temperature or at 6 °C. After the reaction completion, the mixture was washed with water acidified with HCl. The organic layer was dried with anhydrous Na2SO4. The solvent was evaporated under reduced pressure. The reaction products were separated by column chromatography, using chloroform as an eluent.
 

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