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Chemical Structure| 2292-84-4 Chemical Structure| 2292-84-4

Structure of 2292-84-4

Chemical Structure| 2292-84-4

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Product Details of [ 2292-84-4 ]

CAS No. :2292-84-4
Formula : C8H14O2
M.W : 142.20
SMILES Code : O=C1C(C)(C)C(OCC)C1
MDL No. :MFCD18452159

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Application In Synthesis of [ 2292-84-4 ]

* 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 [ 2292-84-4 ]

[ 2292-84-4 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 50593-30-1 ]
  • [ 2292-84-4 ]
  • 7-isopropyl-2-methyl-2H-pyrazolo[3,4-f]quinoline [ No CAS ]
  • 2
  • [ 394-69-4 ]
  • [ 2292-84-4 ]
  • 7-fluoro-4a-hydro-4,4-dimethyl-3H-benzo[c]quinolizin-3-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With trimethylsilyl trifluoromethanesulfonate; In acetonitrile; at 24℃; for 0.333333h; General procedure: To a stirred solution of 5-nitro<strong>[394-69-4]quinoline</strong> (8a, 103 mg, 0.59 mmol) and 2,2-dimethyl-3-ethoxycyclobutanone (7a, 92.5 mg, 0.65 mmol) in dry acetonitrile (2 mL) was addedMe3SiOTf (0.12 mL, 0.65 mmol) at 24 °C and the mixture was stirred for 20 min at the sametemperature. The reaction was quenched by adding aqueous solution of potassium sodium(+)-tartrate and the resulting mixture was extracted with ethyl acetate (three times). The combinedorganic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered, andconcentrated. The crude product was purified by column chromatography on silica gel (13.7 g,hexane/ethyl acetate = 3:1 to 1:1) to afford 9a (101.4 mg, 0.375 mmol, 64percent).
  • 3
  • [ 2292-84-4 ]
  • [ 57297-29-7 ]
  • 2-cyclopropyl-4-isopropylpyrimidine [ No CAS ]
  • 4
  • [ 2292-84-4 ]
  • [ 62980-03-4 ]
  • C14H13F3N2 [ No CAS ]
  • 5
  • [ 2292-84-4 ]
  • [ 62980-03-4 ]
  • 4-(2-nitropropan-2-yl)-2-(3-(trifluoromethyl)phenyl)pyrimidine [ No CAS ]
 

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