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Chemical Structure| 202534-94-9 Chemical Structure| 202534-94-9

Structure of 202534-94-9

Chemical Structure| 202534-94-9

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Product Details of [ 202534-94-9 ]

CAS No. :202534-94-9
Formula : C15H16FNO4
M.W : 293.29
SMILES Code : O=C(C(C(C1=CC=C(F)C=C1)C2)C(N(C)C2=O)=O)OCC
MDL No. :MFCD08436981

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Application In Synthesis of [ 202534-94-9 ]

* 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 [ 202534-94-9 ]

[ 202534-94-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 71510-95-7 ]
  • [ 459-57-4 ]
  • [ 202534-94-9 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; acetic acid; In water; ethyl acetate; EXAMPLE 4 (+-)-trans-3-Ethoxycarbonyl-4-(4'-fluorophenyl)-N-methylpiperidin-2,6-dione (E4) A solution of p-fluorobenzaldehyde (100 g) in ethyl acetate (100 ml) was added slowly to a mixture of sodium methoxide (105 g) in ethyl acetate (900 ml), maintaining the temperature at 10-20 C. and stirring for a further 30 minutes at 15-25 C. Then a solution of desiccated ethyl N-methylamidomalonate (139 g) in ethyl acetate (200 ml) was added over 1 hour whilst maintaining the temperature at 15-25 C. and stirring for a further 1-2 hours. The resulting mixture was added to a solution of acetic acid (120 g) in water (475 ml) and stirred for 15 minutes. The lower aqueous layer was then separated and discarded. The rich solvent was washed with saturated brine (250 ml). The solvent was removed by vacuum distillation and replaced with propan-2-ol then cooled with stirring to obtain the crystalline title compound. Water (600 ml) was added over 30 minutes and the mixture stirred for 1-2 hours at 15-25 C. The product was filtered and washed with water then isopropyl ether before drying.
With sodium methylate; acetic acid; In water; ethyl acetate; Example 4 (+-)-trans-3-Ethoxycarbonyl-4-(4'-fluorophenyl)-N-methyl-piperidin-2,6-dione (E4) A solution of p-fluorobenzaldehyde (100g) in ethyl acetate (100ml) was added slowly to a mixture of sodium methoxide (105g) in ethyl acetate (900ml), maintaining the temperature at 10-20C and stirring for a further 30 minutes at 15-25C. Then a solution of desiccated ethyl N-methylamidomalonate (139g) in ethyl acetate (200ml) was added over 1 hour whilst maintaining the temperature at 15-25C and stirring for a further 1-2 hours. The resulting mixture was added to solution of acetic acid (120g) in water (475ml) and stirred for 15 minutes. The lower aqueous layer was then separated and discarded. The rich solvent was washed with saturated brine (250ml). The solvent was removed by vacuum distillation and replaced with propan-2-ol then cooled with stirring to obtain the crystalline title compound. Water (600ml) was added over 30 minutes and the mixture stirred for 1-2 hours at 15-25C. The product was filtered and washed with water then isopropyl ether before drying. Yield = 80-90%
  • 2
  • [ 71510-95-7 ]
  • C14H13FN2O [ No CAS ]
  • [ 202534-94-9 ]
 

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