(E)-(2-(phenylsulfonyl)vinyl)benzene and derivative thereof, and synthesis method of (E)-(2-(phenylsulfonyl)vinyl)benzene and derivative thereof
A technology of phenylsulfonyl and benzylsulfonyl, which is applied in the field of synthesis of -vinyl)benzene and its derivatives, achieving the effects of less reaction equipment, mild reaction conditions and simple reaction system
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Embodiment 1
[0074] The NMR and mass spectrometry data of embodiment 1 product are as follows:
[0075] 1 H NMR (400MHz, CDCl 3 )δ7.69(d, J=15.4Hz, 1H), 7.65-7.50(m, 4H), 7.52-7.44(m, 2H), 7.44-7.34(m, 3H), 6.88(d, J=15.5Hz , 1H). 13 C NMR (100MHz, CDCl 3 )δ142.4, 140.5, 133.3, 132.1, 131.1, 129.2, 129.0, 128.5, 127.5, 127.0.
Embodiment 2
[0076] The NMR and mass spectrometry data of embodiment 2 product are as follows:
[0077] 1 H NMR (400MHz, CDCl 3 )δ7.95(d, J=8.0Hz, 2H), 7.69-7.52(m, 4H), 7.38(d, J=7.6Hz, 2H), 7.20(d, J=7.7Hz, 2H), 6.81( d, J=15.4Hz, 1H), 2.37(s, 3H). 13 C NMR (100MHz, CDCl 3 )δ142.6, 141.8, 140.9, 133.2, 129.8, 129.7, 129.3, 128.6, 127.6, 126.0, 21.5.
Embodiment 3
[0078] The NMR and mass spectrum data of embodiment 3 product are as follows:
[0079] 1 H NMR (400MHz, CDCl 3 )δ7.95(d, J=7.4Hz, 2H), 7.65(dd, J=15.3, 8.6Hz, 2H), 7.56(t, J=7.5Hz, 2H), 7.47-7.51(m, 2H), 7.09(t, J=8.5Hz, 2H), 6.80(d, J=15.4Hz, 1H). 13 C NMR (100MHz, CDCl 3 )δ164.3 (d, J=251.5Hz), 141.1, 140.5, 133.4, 130.6 (d, J=87.1Hz), 129.4, 128.5 (d, J=3.3Hz), 127.6, 127.0 (d, J=1.9 Hz), 116.3(d, J=21.9Hz).
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