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Chemical Structure| 59292-48-7 Chemical Structure| 59292-48-7

Structure of 59292-48-7

Chemical Structure| 59292-48-7

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Product Details of [ 59292-48-7 ]

CAS No. :59292-48-7
Formula : C5H8N2O
M.W : 112.13
SMILES Code : CCOC1=NNC=C1
MDL No. :MFCD22052967

Safety of [ 59292-48-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 59292-48-7 ]

* 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 [ 59292-48-7 ]

[ 59292-48-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 383-62-0 ]
  • [ 59292-48-7 ]
  • 1-(difluoromethyl)-3-ethoxy-1H-pyrazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 12h; Step 3 - Synthesis of l-(difluoromethyl)-3-ethoxy-lH-pyrazole [0234] To a 100 mL round-bottom flask was added 3-ethoxy-lH-pyrazole (2.0 g, 17.84 mmol, 1.00 equiv), N,N-dimethylformamide (30 mL) and potassium carbonate (4.9 g, 35.45 mmol, 2.00 equiv), followed by the addition of <strong>[383-62-0]ethyl 2-chloro-2,2-difluoroacetate</strong> (3.4 g, 21.45 mmol, 1.20 equiv) dropwise with stirring. The resulting solution was stirred for 12 h at 60 C, then diluted with H20. The resulting mixture was extracted with dichloromethane (3x) and the combined organic layers washed with water, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was applied onto a silica gel column with ethyl ether/hexane (0: 100 to 1 :1) to afford l-(difluoromethyl)-3-ethoxy-lH-pyrazole as a colorless liquid. 1H-NMR (300 MHz, CDC13): delta 7.56 (d, 1H), 7.17 (t, 1H), 5.86 (d, 1H), 4.29 (q, 2H), 1.39 (t, 3H).
With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 12h; [0231] To a 100 mL round-bottom flask was added 3-ethoxy-lH-pyrazole (2.0 g, 17.84 mmol, 1.00 equiv), N,N-dimethylformamide (30 mL) and potassium carbonate (4.9 g, 35.45 mmol, 2.00 equiv), followed by the addition of <strong>[383-62-0]ethyl 2-chloro-2,2-difluoroacetate</strong> (3.4 g, 21.45 mmol, 1.20 equiv) dropwise with stirring. The resulting solution was stirred for 12 h at 60 C, then diluted with H20. The resulting mixture was extracted with dichloromethane (3x) and the combined organic layers washed with water, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was applied onto a silica gel column with ethyl ether/hexane (0: 100 to 1 :1) to afford l-(difluoromethyl)-3-ethoxy-lH-pyrazole as a colorless liquid. 1H-NMR (300 MHz, CDC13): delta 7.56 (d, 1H), 7.17 (t, 1H), 5.86 (d, 1H), 4.29 (q, 2H), 1.39 (t, 3H).
 

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