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[ CAS No. 4472-55-3 ] {[proInfo.proName]}

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Chemical Structure| 4472-55-3
Chemical Structure| 4472-55-3
Structure of 4472-55-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4472-55-3 ]

CAS No. :4472-55-3 MDL No. :MFCD11869966
Formula : C8H10ClN Boiling Point : -
Linear Structure Formula :- InChI Key :VYEFLSRYAXMVDI-UHFFFAOYSA-N
M.W : 155.63 Pubchem ID :13742925
Synonyms :

Safety of [ 4472-55-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4472-55-3 ]

* 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.

  • Upstream synthesis route of [ 4472-55-3 ]
  • Downstream synthetic route of [ 4472-55-3 ]

[ 4472-55-3 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 108-75-8 ]
  • [ 4472-55-3 ]
YieldReaction ConditionsOperation in experiment
28.9% With hydrogenchloride; chlorine In chloroform; trichloroisocyanuric acid; ethyl acetate EXAMPLE 7
2-chloromethyl-4,6-dimethyl-pyridine
A solution of 121.18 g (1 mole) of 2,4,6-collidine in 400 ml of chloroform was heated at reflux while adding in portions 140 g (0.6 mole) of trichloroisocyanuric acid (min. 90percent available chlorine) over 4 hours and stirring was continued for another 30 minutes and then cooled and filtered.
The filtrate was admixed with 150 ml of 10percent HCl to transform the product into the aqueous phase.
The decanted acid aqueous phase was mixed with 150 ml of ethyl acetate and was made alkaline with sodium hydroxide.
The decanted aqueous phase was extracted with 100 ml of ethyl acetate.
The organic phase was dried and evaporated to dryness under reduced pressure to obtain 45 g (28.9percent) of 2-chloromethyl-4,6-dimethyl pyridine with a Cl content of 22.78percent (theoretical 22.78percent) and a boiling point of 64° to 70° C. at 1 mm Hg.
Reference: [1] Chemische Berichte, 1987, vol. 120, p. 649 - 652
[2] Patent: US4719298, 1988, A,
  • 2
  • [ 3376-50-9 ]
  • [ 4472-55-3 ]
  • [ 120739-87-9 ]
Reference: [1] Synthetic Communications, 2004, vol. 34, # 6, p. 1097 - 1103
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