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Chemical Structure| 1006950-51-1 Chemical Structure| 1006950-51-1

Structure of 1006950-51-1

Chemical Structure| 1006950-51-1

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Product Details of [ 1006950-51-1 ]

CAS No. :1006950-51-1
Formula : C6H9N3O3
M.W : 171.15
SMILES Code : O=[N+](C1=NN(CCO)C(C)=C1)[O-]
MDL No. :MFCD06804921

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Application In Synthesis of [ 1006950-51-1 ]

* 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 [ 1006950-51-1 ]

[ 1006950-51-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 624-76-0 ]
  • [ 34334-96-8 ]
  • [ 1006950-51-1 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In acetonitrile; for 18h;Reflux; A solution of 5-methyl-3-nitro-lH-pyrazole (500 mg, 3.93 mmol) and potassium carbonate (1.08 g, 7.81 mmol) in acetonitrile (20 mL) was treated dropwise with 2- iodoethanol (2.00 g, 1 1.6 mmol) and the reaction stirred at reflux for 18 h. After this time, the reaction was cooled to room temperature, diluted with ethyl acetate (100 mL) and filtered through diatomaceous earth. The filtrate was concentrated under reduced pressure and the resulting residue purified by chromatography (silica, gradient, heptane to 1 : 1 ethyl acetate/heptane) to afford 2-(5-methyl-3-nitro-lH-pyrazol-l-yl)ethanol as a white solid: NMR (400 MHz, DMSO-i¾d 6.82 (s, 1H), 4.97 (t, J = 5.2 Hz, 1H), 4.19 (t, J = 5.2 Hz, 2H), 3.75 (q, J= 5.2 Hz, 2H), 2.35 (s, 3H).
With potassium carbonate; In acetonitrile; for 18h;Reflux; Example 7 Preparation of 2-(5-methyl-3-nitro-1H-pyrazol-1-yl)ethanol A solution of <strong>[34334-96-8]5-methyl-3-nitro-1H-pyrazole</strong> (500 mg, 3.93 mmol) and potassium carbonate (1.08 g, 7.81 mmol) in acetonitrile (20 mL) was treated dropwise with 2-iodoethanol (2.00 g, 11.6 mmol) and the reaction stirred at reflux for 18 h. After this time, the reaction was cooled to room temperature, diluted with ethyl acetate (100 mL) and filtered through diatomaceous earth. The filtrate was concentrated under reduced pressure and the resulting residue purified by chromatography (silica, gradient, heptane to 1:1 ethyl acetate/heptane) to afford 2-(5-methyl-3-nitro-1H-pyrazol-1-yl)ethanol as a white solid: 1H NMR (400 MHz, DMSO-d6.) d 6.82 (s, 1H), 4.97 (t, J=5.2 Hz, 1H), 4.19 (t, J=5.2 Hz, 2H), 3.75 (q, J=5.2 Hz, 2H), 2.35 (s, 3H).
 

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