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Chemical Structure| 2622-72-2 Chemical Structure| 2622-72-2

Structure of 2622-72-2

Chemical Structure| 2622-72-2

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Product Details of [ 2622-72-2 ]

CAS No. :2622-72-2
Formula : C14H11ClN2
M.W : 242.70
SMILES Code : CN1C(C2=CC=C(Cl)C=C2)=NC3=CC=CC=C31

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Application In Synthesis of [ 2622-72-2 ]

* 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 [ 2622-72-2 ]

[ 2622-72-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1019-85-8 ]
  • [ 74-88-4 ]
  • [ 2622-72-2 ]
YieldReaction ConditionsOperation in experiment
98.3% BD-C; A mixture of <strong>[1019-85-8]2-(4-chlorophenyl)benzimidazole</strong> (17.1 g, 0.075 mole), crushed KOH (12.6 g, 0.225 mole and DMSO (40 mL) was added to a reaction flask and stirred for 20 minutes at 20-25 C. Methyl iodide (7.0 mL, 0112 mole) was added dropwise over a period of 20 minutes, the thickened mixture was diluted with water. The product was filtered, washed with water, squeezed, vacuum filtered, and dried at 60-80 C. yielding 17.84 g (98.3%). An NMR spectrum showed the product to have a structure consistent with 2-(4-chlorophenyl)-1-methylbenzimidazole.
98.3% A mixture of 2- (4-chlorophenyl)benzimidazole (17.1 g, 0.075 mole), crushed KOH (12.6 g, 0.225 mole and DMSO (40 mL) was added to a reaction flask and stirred for 20 minutes at 20-25 0C. Methyl iodide (7.0 mL, 0112 mole) was added dropwise over a period of 20 minutes, the thickened mixture was diluted with water. The product was filtered, washed with water, squeezed, vacuum filtered, and dried at 60-80 0C yielding 17.84 g (98.3%). An NMR spectrum showed the product to have a structure consistent with 2- (4-chlorophenyl) -1-methylbenzimidazole.
 

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