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Chemical Structure| 26583-71-1 Chemical Structure| 26583-71-1

Structure of 26583-71-1

Chemical Structure| 26583-71-1

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Product Details of [ 26583-71-1 ]

CAS No. :26583-71-1
Formula : C11H17NO
M.W : 179.26
SMILES Code : CC(OC1=C(C)C=CC=C1C)CN

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Application In Synthesis of [ 26583-71-1 ]

* 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 [ 26583-71-1 ]

[ 26583-71-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5926-51-2 ]
  • [ 26583-71-1 ]
  • [{2-methyl-2-(2,6-dimethylphenoxy)}ethyl]-3-bromomaleimide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium acetate; In tetrahydrofuran; acetic acid; ethyl acetate; EXAMPLE 2 (PROCESS B) Production of [{2-methyl-2-(2,6-dimethylphenoxy)}ethyl]-3-bromomaleimide (Compound No. 6) In 10 ml of tetrahydrofuran were dissolved 0.7 g of [2-methyl-2-(2,6-dimethylphenoxy)]ethylamine and 0.76 g of 3-<strong>[5926-51-2]bromomaleic anhydride</strong>, and the solution was heated and refluxed for 1 hour. The reaction liquid was concentrated under a reduced pressure and the obtained residue was dissolved in 5 ml of anhydrous acetic acid, 20 mg of sodium acetate was added to the solution, and the reaction was carried out at 100° C. for 3 hours. The reaction liquid was concentrated under a reduced pressure and the residue was dissolved in ethyl acetate, washed with water, and dried with magnesium sulfate. The solvent was then removed by distillation. The obtained residue was purified by silica gel chromatography [eluted with n-hexane/ethyl acetate (9/1)] to obtain 0.72 g of the intended compound.
With sodium acetate; In tetrahydrofuran; acetic acid; ethyl acetate; Example 2 (Process B) Production of [{2-methyl-2-(2,6-dimethylphenoxy)}ethyl]-3-bromomaleimide (Compound No. 6) In 10 ml of tetrahydrofuran were dissolved 0.7 g of [2-methyl-2-(2,6-dimethylphenoxy)]ethylamine and 0.76 g of 3-<strong>[5926-51-2]bromomaleic anhydride</strong>, and the solution was heated and refluxed for 1 hour. The reaction liquid was concentrated under a reduced pressure and the obtained residue was dissolved in 5 ml of anhydrous acetic acid, 20 mg of sodium acetate was added to the solution, and the reaction was carried out at 100°C for 3 hours. The reaction liquid was concentrated under a reduced pressure and the residue was dissolved in ethyl acetate, washed with water, and dried with magnesium sulfate. The solvent was then removed by distillation. The obtained residue was purified by silica gel chromatography [eluted with n-hexane/ethyl acetate (9/1)] to obtain 0.72 g of the intended compound.
 

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