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Chemical Structure| 93749-47-4 Chemical Structure| 93749-47-4

Structure of 93749-47-4

Chemical Structure| 93749-47-4

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Product Details of [ 93749-47-4 ]

CAS No. :93749-47-4
Formula : C14H20O5
M.W : 268.31
SMILES Code : O=C(OC)C1=CC=C(OCC(OCC)OCC)C=C1
MDL No. :MFCD03695469

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Application In Synthesis of [ 93749-47-4 ]

* 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 [ 93749-47-4 ]

[ 93749-47-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1075-35-0 ]
  • [ 93749-47-4 ]
  • [ 479422-23-6 ]
YieldReaction ConditionsOperation in experiment
92% With triethylsilane; trifluoroacetic acid; In dichloromethane; water; at 20℃; for 48h; To the above product (1.0 eq) and 5-chloro-2-methyl indole (1.0 eq) in CH2Cl2 (0.12 M) was added triethylsilane (3.0 eq) followed by trifluoroacetic acid (3.0 eq). After being stirred overnight at room temperature, added water and trifluroacetic acid (1.0 eq) to the reaction mixture, stirred at room temperature for two days, diluted with CH2Cl2, washed with 1N NaOH, water, brine, dried over sodium sulfate. Trituration of the material with CH2Cl2 and hexanes afforded the C3 alkylated indole in 92% yield
92% To the above product (1.0 eq) and 5-chloro-2-methyl indole (1.0 eq) in CH2CI2 (0.12 M) was added triethylsilane (3.0 eq) followed by trifluoroacetic acid (3.0 eq). After being stirred overnight at room temperature, water and trifluroacetic acid (1.0 eq) were added to the reaction mixture, which was stirred at room temperature for two days, diluted with CH2CI2, washed with 1N NaOH, water, and brine, and dried over sodium sulfate. Trituration of the material with CH2CI2 and hexanes afforded the C3 alkylated indole in 92% yield
92% With triethylsilane; trifluoroacetic acid; In dichloromethane; at 20℃; To the above product (1.0 eq) and 5-chloro-2-methyl indole (1.0 eq) in CH2Cl2 (0.12 M) was added triethylsilane (3.0 eq) followed by trifluoroacetic acid (3.0 eq). After being stirred overnight at room temperature, added water and trifluroacetic acid (1.0 eq) to the reaction mixture, stirred at room temperature for two days, diluted with CH2Cl2, washed with 1N NaOH, water, brine, dried over sodium sulfate. Trituration of the material with CH2Cl2 and hexanes afforded the C3 alkylated indole in 92% yield
 

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