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Chemical Structure| 119778-43-7 Chemical Structure| 119778-43-7

Structure of 119778-43-7

Chemical Structure| 119778-43-7

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Product Details of [ 119778-43-7 ]

CAS No. :119778-43-7
Formula : C6H6ClNOS
M.W : 175.64
SMILES Code : O=C(Cl)C1=C(C)N=C(C)S1
MDL No. :MFCD26401247

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Application In Synthesis of [ 119778-43-7 ]

* 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 [ 119778-43-7 ]

[ 119778-43-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 53137-27-2 ]
  • [ 119778-43-7 ]
YieldReaction ConditionsOperation in experiment
95.0% and 98.0% In 5,5-dimethyl-1,3-cyclohexadiene; EXAMPLE 1 In a 300-ml three-neck flask, 7.9 g (0.5) mole) of 2,4-dimethylthiazole-5carboxylic acid were suspended in 200 ml of xylene and under heating and reflux, phosgene was blown at a flow rate of 340 ml/hr for 12 hours (0.18 mole). After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated to obtain 8.2 g of <strong>[53137-27-2]2,4-dimethylthiazole-5-carboxylic acid</strong> chloride. Its purity and yield were 95.0% and 98.0%, respectively.
97.5% and 98.0% In N,N-dimethyl-formamide; toluene; EXAMPLE 10 In a similar apparatus to Example 1, 15.7 g (0.1 mole) of <strong>[53137-27-2]2,4-dimethylthiazole-5-carboxylic acid</strong> were suspended in 100 ml of toluene, followed by the addition of 0.1 g of N,N-dimethylformamide. Under heating and reflux, phosgene was blown at a rate of 1.3 l/hr for 5 hours (0.29 mole). After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated to obtain 17.2 g of <strong>[53137-27-2]2,4-dimethylthiazole-5-carboxylic acid</strong> chloride. Its purity and yield were 97.5% and 98.0%, respectively.
With thionyl chloride; In dichloromethane; at 20℃; for 1h; The <strong>[53137-27-2]2,4-dimethyl-thiazole-5-carboxylic acid</strong> (50.0mg, 0.318mmol) and dichloromethane (2mL) into 10mL round bottom flask at 0 was added thionyl chloride (378.43mg, 3.18 mmol) was stirred at room temperature for 1 hour. TLC showed the reaction was complete. The mixture was concentrated to give the title compound as a black solid, used without purification in the next reaction.
 

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