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Chemical Structure| 944407-72-1 Chemical Structure| 944407-72-1

Structure of 944407-72-1

Chemical Structure| 944407-72-1

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Product Details of [ 944407-72-1 ]

CAS No. :944407-72-1
Formula : C13H22ClNO2Si
M.W : 287.86
SMILES Code : COC1=CC(CO[Si](C)(C(C)(C)C)C)=CC(Cl)=N1

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Application In Synthesis of [ 944407-72-1 ]

* 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 [ 944407-72-1 ]

[ 944407-72-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 18162-48-6 ]
  • [ 193001-91-1 ]
  • [ 944407-72-1 ]
YieldReaction ConditionsOperation in experiment
93% With 1H-imidazole; In N,N-dimethyl-formamide; at 20℃; for 2h; (a) 2-Chloro-4-([(l,l-dimethylethyl)(dimethyl)silyl]oxy}methyl)-6-(methyloxy)pyridineA solution of <strong>[193001-91-1][2-chloro-6-(methyloxy)-4-pyridinyl]methanol</strong> (for a synthesis see Adamczyk, M.; Akireddy, S. R.; Reddy, Rajarathnam E. Tetrahedron 2002, 58(34), 6951)(8.02 g, 46.22 mmol) in dry DMF (100 ml) was treated with tert-butyldimethylsilyl chloride (8.36 g, 55.46 mmol) and imidazole (3.77 g, 55.46 mmol) and stirred at rt for 2h. The reaction mixture was treated with water extracted three times with dichloromethane, <n="75"/>dried (magnesium sulphate), evaporated and chromatographed on silica gel (100 g), eluting with 1 :4 ethyl acetate-hexane to give the desired product (12.38g, 93%). MS (+ve ion electrospray) m/z 288/290 (MH+).
93% With 1H-imidazole; In N,N-dimethyl-formamide; at 20℃; for 2h; (a) 2-Chloro-4-([(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-6-(methyloxy)pyridine A solution of <strong>[193001-91-1][2-chloro-6-(methyloxy)-4-pyridinyl]methanol</strong> (for a synthesis, see Adamczyk, M.; Akireddy, S. R.; Reddy, Rajarathnam E. Tetrahedron 2002, 58(34), 6951)(8.02 g, 46.22 mmol) in dry dimethylformamide (100 ml) was treated with tert-butyldimethylsilyl chloride (8.36 g, 55.46 mmol) and imidazole (3.77 g, 55.46 mmol) and stirred at room temperature for 2 hours. The reaction mixture was treated with water extracted 3* with dichloromethane, dried (magnesium sulphate), evaporated and chromatographed on silica gel (100 g), eluding with 1:4 ethyl acetate-hexane to give the desired product (12.38 g, 93%). MS (+ve ion electrospray) m/z 288/290 (MH+).
  • 2
  • [ 288-32-4 ]
  • [ 18162-48-6 ]
  • [ 141-78-6 ]
  • [ 193001-91-1 ]
  • [ 944407-72-1 ]
YieldReaction ConditionsOperation in experiment
93% In N-methyl-acetamide; water; (a) 2-Chloro-4-([(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-6-(methyloxy)pyridine A solution of <strong>[193001-91-1][2-chloro-6-(methyloxy)-4-pyridinyl]methanol</strong> (for a synthesis, see)(8.02 g, 46.22 mmol) in dry dimethylformamide (100 ml) was treated with tert-butyldimethylsilyl chloride (8.36 g, 55.46 mmol) and imidazole (3.77 g, 55.46 mmol) and stirred at room temperature for 2 hours. The reaction mixture was treated with water extracted 3x with dichloromethane, dried (magnesium sulphate), evaporated and chromatographed on silica gel (100 g), eluding with 1:4 ethyl acetate-hexane to give the desired product (12.38 g, 93%). MS (+ve ion electrospray) m/z 288/290 (MH+).
 

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