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Chemical Structure| 302561-09-7 Chemical Structure| 302561-09-7

Structure of 302561-09-7

Chemical Structure| 302561-09-7

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Product Details of [ 302561-09-7 ]

CAS No. :302561-09-7
Formula : C12H17NO2S
M.W : 239.33
SMILES Code : O=C(C1=C(N)SC2=C1CCCC2)OCCC
MDL No. :MFCD00449584

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Application In Synthesis of [ 302561-09-7 ]

* 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 [ 302561-09-7 ]

[ 302561-09-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14447-15-5 ]
  • [ 108-94-1 ]
  • [ 302561-09-7 ]
YieldReaction ConditionsOperation in experiment
91% With sulfur; diethylamine; In methanol; ethanol; at 20℃;Sonication; General procedure: Compound C was synthesized following to the procedure ofGewald et al. [22], as already reported with some minor modifications[21]. The mixture of ketone D (1 mmol), alkyl cyanoacetateE (1.1 mmol), sulfur (1.1 mmol), and diethylamine (1.1 mmol) inethanol/methanol (10 mL) was kept at room temperature in anultrasonic cleaner for 1-3 h. After completion of the reaction, thesolvent was evaporated to dryness under reduced pressure. Thecrude product was purified by flash column chromatography onsilica gel (petroleum ether/ethyl acetate elute) to provide theproduct C.
With sulfur; diethylamine; In DMF (N,N-dimethyl-formamide); at 60℃; for 2h; To n-<strong>[14447-15-5]propyl cyanoacetate</strong> (2.54 g, 20 mmol) and sulfur (0.64 g) in DMF (4 mL), diethylamine (1.6 mL) is added under stirring. To this solution cyclohexanone (2.03 g, 20 mmol) is added dropwise. The mixture is heated to [60 C] for 2 hours and it is poured into water (30 mL), which is extracted with diethyl ether (30 mL). The ethereal solution is dried with sodium sulfate and concentrated to give the desired compound as an orange solid (2.85 g). Physical characteristics: MS (ES+) [FOR M/Z] 240.
 

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