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Chemical Structure| 1089212-37-2 Chemical Structure| 1089212-37-2

Structure of 1089212-37-2

Chemical Structure| 1089212-37-2

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Product Details of [ 1089212-37-2 ]

CAS No. :1089212-37-2
Formula : C5H6F2N2
M.W : 132.11
SMILES Code : CN1N=C(C(F)F)C=C1
MDL No. :MFCD21668139

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Application In Synthesis of [ 1089212-37-2 ]

* 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 [ 1089212-37-2 ]

[ 1089212-37-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27258-32-8 ]
  • [ 1089212-37-2 ]
YieldReaction ConditionsOperation in experiment
66.8% With diethylamino-sulfur trifluoride; In dichloromethane; at -20 - 20℃; 17. Preparation of 3-difluoromethyl-1-methylpyrazole from <strong>[27258-32-8]1-methylpyrazole-3-carbaldehyde</strong>At -20° C., (diethylamino)sulfur trifluoride (DAST, 87.8 g, 0.54 mol) was added dropwise to a solution of <strong>[27258-32-8]1-methylpyrazole-3-carbaldehyde</strong> (20 g, 0.18 mol) in methylene chloride (200 ml). The reaction mixture was stirred at room temperature overnight. The reaction mixture was then added carefully to ice/water (400 g) and extracted twice with methylene chloride (100 ml each). The combined organic phase was washed twice with water (100 ml each) and twice with NaCl solution (100 ml each) and dried over magnesium sulfate, and the solvent was removed under reduced pressure. The residue was separated by fractional distillation. 3-Difluoromethyl-1-methylpyrazole (16.5 g, transition temperature 141° C. at 570 mbar) was isolated in a purity of 95percent. This corresponds to a yield of 66.8percent.
With diethylamino-sulfur trifluoride; In dichloromethane; at 0 - 20℃; To a solution of <strong>[27258-32-8]1-methyl-1H-pyrazole-3-carbaldehyde</strong> (4.00 g, 36.33 mmol) in CH2Cl2 (50 mL) at 0° C. was added DAST (23.4 g, 145.17 mmol, 4.00 equiv) dropwise. The reaction mixture was stirred overnight at room temperature and then was quenched by the addition of saturated NaHCO3 (100 mL), and extracted with CH2Cl2 (3×200 mL). The combined organic layers were dried over anhydrous MgSO4, filtered and concentrated to provide the desired product as an oil (4.8 g, crude) which was used in the next reaction without further purification. 1H NMR (400 MHz, CDCl3): delta 7.32-7.37 (m, 1H), 6.44-6.45 (t, 1H), 6.80 (m, 1H), 3.90 (s, 3H) ppm.
 

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