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Chemical Structure| 63876-46-0 Chemical Structure| 63876-46-0

Structure of 63876-46-0

Chemical Structure| 63876-46-0

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Product Details of [ 63876-46-0 ]

CAS No. :63876-46-0
Formula : C10H12O3
M.W : 180.20
SMILES Code : CCC(C1=CC=C(O)C(C)=C1O)=O
MDL No. :MFCD00010818

Safety of [ 63876-46-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 63876-46-0 ]

* 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 [ 63876-46-0 ]

[ 63876-46-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 39796-52-6 ]
  • [ 63876-46-0 ]
  • C19H22N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
17% In dimethyl sulfoxide; at 100℃; for 22h; 127 (120 mg, 0.72 mmol) obtained as mentioned above, k-1 (100 mg, 0.55 mmol) were dissolved in DMSO (1.1 mL), and the mixture was stirred at 100 C. for 22 hr. The mixture was allowed to cool, and the reaction solution was directly purified by moderate-pressure silica gel column chromatography (silica gel 10 g, ethyl acetate/hexane=10/90-80/20). The obtained solid was washed with IPE, methylene chloride, and dried under reduced pressure to give k-1:C-2 (29.9 mg, 0.0908 mmol, yield 17%) as a yellow solid. 1H-NMR (400 MHz):δ9.63 (s, 1H), 8.55 (m, NH), 7.40-7.20 (m, 6H), 6.25 (d, J=8.0 Hz, 1H), 4.32 (d, J=8.0 Hz, 2H), 4.29 (s, 2H), 2.70 (q, J=8.0 Hz, 2H), 1.91 (s, 3H), 1.09 (t, J=8.0 Hz, 3H).(one signal of OH was not observed)
17% In dimethyl sulfoxide; at 100℃; for 22h; 127 (120 mg, 0.72 mmol) obtained as mentioned above, k-1 (100 mg, 0.55 mmol) were dissolved in DMSO(1.1 mL), and the mixture was stirred at 100C for 22 hr. The mixture was allowed to cool, and the reaction solution wasdirectly purified by moderate-pressure silica gel column chromatography (silica gel 10 g, ethyl acetate/hexane=10/90 -80/20). The obtained solid was washed with IPE, methylene chloride, and dried under reduced pressure to give k-1:C-2 (29.9 mg, 0.0908 mmol, yield 17%) as a yellow solid.1H-NMR (400 MHz):δ9.63 (s, 1H), 8.55(m, NH), 7.40-7.20(m, 6H), 6.25(d, J=8.0Hz, 1H), 4.32(d, J=8.0Hz, 2H), 4.29(s,2H), 2.70(q, J=8.0Hz, 2H), 1.91(s, 3H), 1.09(t, J=8.0Hz, 3H).(one signal of OH was not observed)
 

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