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Chemical Structure| 166978-61-6 Chemical Structure| 166978-61-6

Structure of 166978-61-6

Chemical Structure| 166978-61-6

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Product Details of [ 166978-61-6 ]

CAS No. :166978-61-6
Formula : C13H14O3
M.W : 218.25
SMILES Code : O=C(C1=CC2=C(C(C)(C)CC2=O)C=C1)OC

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Application In Synthesis of [ 166978-61-6 ]

* 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 [ 166978-61-6 ]

[ 166978-61-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38222-83-2 ]
  • [ 166978-61-6 ]
  • [ 60-29-7 ]
  • [ 166978-62-7 ]
YieldReaction ConditionsOperation in experiment
85% In dichloromethane; EXAMPLE 125 Methyl 1,1-dimethyl-3-(trifluoromethanesulfonyloxy)-1H-indene-5-carboxylate STR119 To a solution of methyl 1,1-dimethyl-3-oxo-indan-5-carboxylate (0.90 g, 4.12 mmol) and <strong>[38222-83-2]2,6-di-tert-butyl-4-methylpyridine</strong> (1.10 mg, 5.36 mmol) in 10 mL of methylene chloride was added triflic acid anhydride (1.39 g, 4.94 mmol) at -78° C. After being stirred at room temperature for 16 hours, the mixture was diluted with 70 mL of ethyl ether, washed with 1N HCl (20 mL), dried over magnesium sulfate, and evaporated. The residue was purified by flash chromatography (EtOAc:hexane=1:20 to 1:5) to give 1.23 g (85percent yield) of the title compound; 1 H NMR (CDCl3) delta1.41 (s, 6H),3.95 (s, 3H), 6.30 (s, 1H), 7.44 (d, J=7.8 Hz, 1H), 7.99 (s, 1H), 8.06 (d, J=7.8 Hz, 1H); MS m/e 351 (MH+).
85% In dichloromethane; EXAMPLE 125 Methyl 1,1-dimethyl-3-(trifluoromethanesulfonyloxy)-1H-indene-5-carboxylate STR119 To a solution of methyl 1,1-dimethyl-3-oxo-indan-5-carboxylate (0.90 g, 4.12 mmol) and <strong>[38222-83-2]2,6-di-tert-butyl-4-methylpyridine</strong> (1.10 mg, 5.36 mmol) in 10 mL of methylene chloride was added triflic acid anhydride (1.39 g, 4.94 mmol) at -78° C. After being stirred at room temperature for 16 hours, the mixture was diluted with 70 mL of ethyl ether, washed with 1N HCl (20 mL), dried over magnesium sulfate, and evaporated. The residue was purified by flash chromatography (EtOAc:hexane=1:20 to 1:5) to give 1.23 g (85percent yield) of the title compound; 1 H NMR (CDCl3) delta 1.41 (s, 6H),3.95 (s, 3H), 6.30 (s, 1H), 7.44 (d, J=7.8 Hz, 1H), 7.99 (s, 1H), 8.06 (d, J=7.8 Hz, 1H); MS m/e 351 (MH+).
 

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