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Chemical Structure| 117724-62-6 Chemical Structure| 117724-62-6

Structure of 117724-62-6

Chemical Structure| 117724-62-6

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Product Details of [ 117724-62-6 ]

CAS No. :117724-62-6
Formula : C8H8F3NO2S
M.W : 239.22
SMILES Code : O=C(C1=C(C(F)(F)F)N=C(C)S1)OCC
MDL No. :MFCD00153150

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Application In Synthesis of [ 117724-62-6 ]

* 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 [ 117724-62-6 ]

[ 117724-62-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 117724-62-6 ]
  • [ 117724-63-7 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; REFERENCE EXAMPLE 2 Synthesis of 2-methyl-4-trifluoromethylthiazole-5-carboxylic acid 1.3 g of ethyl 2-methyl-4-trifluoromethylthiazole-5-carboxylate and 0.4 g of potassium hydroxide were dissolved in a mixture of 5 ml each of water and ethanol and reaction was effected at room temperature overnight. After the reaction, the reaction mixture was concentrated and acidified with dilute hydrochloric acid and extracted with ethyl acetate. The extract was concentrated to obtain 0.89 g of 2-methyl-4-trifluoromethylthiazole-5-carboxylic acid.
21.5 g With sodium hydroxide; In ethyl acetate; at 40℃; for 1h; 115 g of ethyl 2-methyl-4- (trifluoromethyl) thiazole-5-carboxylate (0.102 mol)Of ethyl acetate solution,50 g of a 40% sodium hydroxide solution was added dropwise to the reaction vessel at room temperature,Dropping speed was controlled so that the internal temperature of the system was lower than 40 C,After the dropwise addition of the sodium hydroxide solution,Insulation reaction 60min.After heat preservation,Taking the organic phase,To this was slowly added 10% hydrochloric acid,Adjusted to the system PH ? 2,At this point a large number of estimates of precipitation,The product was filtered,The filter cake was washed twice with 10% hydrochloric acid and dried in a vacuum oven.Methyl-4- (trifluoromethyl) thiazole-5-carboxylic acid as a light yellow solid, 21.5 g of 2-methyl-4- (trifluoromethyl) 98.8%, and the reaction yield was 98.70%.
 

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