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Chemical Structure| 154312-86-4 Chemical Structure| 154312-86-4

Structure of 154312-86-4

Chemical Structure| 154312-86-4

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Product Details of [ 154312-86-4 ]

CAS No. :154312-86-4
Formula : C5H8Cl2N2
M.W : 167.04
SMILES Code : CN1N=CC(CCl)=C1.[H]Cl
MDL No. :MFCD19104829

Safety of [ 154312-86-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 154312-86-4 ]

* 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 [ 154312-86-4 ]

[ 154312-86-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 112029-98-8 ]
  • [ 154312-86-4 ]
YieldReaction ConditionsOperation in experiment
99% With thionyl chloride; In dichloromethane; at 25 - 30℃; for 2h;Inert atmosphere; Cooling; To a cooled solution of <strong>[112029-98-8](1-methyl-1H-pyrazol-4-yl)-methanol</strong> (8.61 g, 0.076 mole) in DCM (100 mL) under N2 atmosphere, thionyl chloride (8.7 mL, 0.12 mole) was added drop wise. The reaction mixture was warmed to RT and stirred for 2 hours. The reaction mixture was concentrated under vacuum at 23 ? 25 °C to obtain the titlecompound.Yield: 12.77 g (99 percent); ?H - NMR (DMSO-d6, 400 MHz) oe ppm: 3.85 (s, 3H), 4.67 (s, 2H), 4.76 - 4.79 (t, 1H), 4.88 (bs, 1H), 7.47 (s, 1H), 7.78 (s, 1H).
With thionyl chloride; In dichloromethane; at 0 - 20℃; for 2h; The compound of formula X (0.201 g, 1.80 mmol) > was dissolved in anhydrous dichloromethane (3 mL) and thionyl chloride (0.140 <n="32"/>ITiL, 1.92 mmol, 1.06 equiv.) was added drop-wise at 0 0C. The reaction was stirred 1 hour at 0 0C and then 1 hour at room temperature. The reaction was then concentrated at 50 0C and dried under vacuum for 2 hours to yield a white solid (0.286 g). This solid was suspended in anhydrous acetonitrile and triethylamine (0.750 ml_, 5.38 mmol, 2.99 equiv.) was added. After stirring for a few minutes, tetraethylammonium cyanide (1.08 g, 6.90 mmol, 3.84 equiv.) was added in one portion. The reaction was stirred 18 hours at room temperature and was then diluted with water (15 ml_) and extracted with ethyl acetate (3 x 20 ml_). The extracts were combined, washed with saturated aqueous sodium chloride, dried over sodium sulfate, filtered and concentrated to yield a yellow oil (0.128 g). Purification by chromatography, eluting with 5percent methanol- dichloromethane, yielded the compound of formula Xl as a yellow oil (0.063 g, 30percent yield).
 

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