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Chemical Structure| 40430-57-7 Chemical Structure| 40430-57-7

Structure of 40430-57-7

Chemical Structure| 40430-57-7

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Product Details of [ 40430-57-7 ]

CAS No. :40430-57-7
Formula : C14H22O
M.W : 206.32
SMILES Code : CC1(C2)CC3(C)CC2(C(C)=O)CC(C3)C1
MDL No. :MFCD01846978

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Application In Synthesis of [ 40430-57-7 ]

* 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 [ 40430-57-7 ]

[ 40430-57-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 702-79-4 ]
  • [ 431-03-8 ]
  • [ 40430-57-7 ]
  • 2
  • [ 702-79-4 ]
  • [ 40430-57-7 ]
YieldReaction ConditionsOperation in experiment
27% EXAMPLE 19 The procedure of Example 18 was repeated, except that the reaction temperature and amount of N-hydroxyphthalimide were changed to 85 C. and 0.6 mmol, respectively, to give 1-acetyl-3,5-dimethyladamantane (yield 41%), 1-acetyl-3,5-dimethyl-7-adamantanol (yield 11%), and 1,3-d-acetyl-5,7-dimethyladamantane (yield 27%), at a conversion rate of <strong>[702-79-4]1,3-dimethyladamantane</strong> of 100%.
5% EXAMPLE 9 Except that the amount of biacetyl was changed to 18 mmol, the procedure of Example 8 was repeated to give 1-acetyl-3,5-dimethyladamantane (yield 18%, selectivity 29%), 1,3-diacetyl-5,7-dimethyladamantane (trace), 1-acetyl-3,5-dimethyl-7-adamantanol (yield 2%, selectivity 3%), 1,3-dimethyl-5-adamantanol (yield 24%, selectivity 38%), and 1,3-dimethyl-4-adamantanone (yield 5%, selectivity 38%), at a conversion rate from <strong>[702-79-4]1,3-dimethyladamantane</strong> of 63%.
5% EXAMPLE 10 Except that the amount of N-hydroxyphthalimide was changed to 0.6 mmol, the procedure of Example 9 was repeated to give 1-acetyl-3,5-dimethyladamantane (yield 32%, selectivity 54%), 1,3-diacetyl-5,7-dimethyladamantane (yield 2%, selectivity 3%), 1-acetyl-3,5-dimethyl-7-adamantanol (yield %, selectivity 2%), 1,3-dimethyl-5-adamantanol (yield 7%, selectivity 12%), and 1,3-dimethyl-4-adamantanone (yield 5%, selectivity 8%), at a conversion rate from <strong>[702-79-4]1,3-dimethyladamantane</strong> of 59%.
 

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