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Chemical Structure| 14994-16-2 Chemical Structure| 14994-16-2

Structure of 14994-16-2

Chemical Structure| 14994-16-2

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Product Details of [ 14994-16-2 ]

CAS No. :14994-16-2
Formula : C8H8ClF
M.W : 158.60
SMILES Code : CC1=CC(F)=CC(C)=C1Cl
MDL No. :MFCD04972723

Safety of [ 14994-16-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 14994-16-2 ]

* 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 [ 14994-16-2 ]

[ 14994-16-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 461-97-2 ]
  • [ 14994-16-2 ]
YieldReaction ConditionsOperation in experiment
With chlorine; iron(III) chloride; a) solvent-free 1 g of anhydrous iron(III) chloride are introduced into 124 g of <strong>[461-97-2]3,5-dimethyl-fluorobenzene</strong> and chlorine is passed in at the rate (about 4 h) at which the reaction proceeds. This is initially somewhat exothermic (temperature rise from 24 to 32° C.) and is kept below 30° C. by cooling. After addition of 120 g of chlorine, the mixture becomes solid. According to GC analysis, 33.4percent of monochloro compound, 58.4percent of desired product and 5percent of overchlorinated compounds are formed. The hydrogen chloride is stripped off and the reaction mixture is then distilled on a column in a water-jet vacuum: 49 g of 2-chloro-<strong>[461-97-2]5-fluoro-1,3-dimethylbenzene</strong> are obtained in the forerun at 72-74° C./22 mbar.
With chlorine; iron(III) chloride; In 1,2-dichloro-ethane; b) in 1,2-dichloroethane 1 kg of <strong>[461-97-2]3,5-dimethyl-fluorobenzene</strong> and 15 g of anhydrous iron(III) chloride were introduced into 1 l of 1,2-dichloroethane, and chlorine was introduced at the rate of the reaction (about 4 h). The reaction is initially slightly exothermic (temperature increase from 24 to 32° C.) and was maintained below 30° C. by gentle cooling. After 1200 g of chlorine had been absorbed, according to GC analysis, 4percent of monochlorinated compound, 81.1percent of desired product and 13.3percent of superchlorinated compounds had formed. After the solvent and hydrogen chloride had been distilled off, distillation was carried out in a waterjet vacuum on a column. In the initial fraction, 40 g of 2-chloro-<strong>[461-97-2]5-fluoro-1,3-dimethylbenzene</strong> were obtained.
 

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