Chem. J. Chinese Universities ›› 2022, Vol. 43 ›› Issue (2): 20210588.doi: 10.7503/cjcu20210588
• Organic Chemistry • Previous Articles Next Articles
YU Jing, WU Chao, LI Chenyang, CHEN Danfeng, DING Liuyue, MA Xiantao()
Received:
2021-08-16
Online:
2022-02-10
Published:
2021-10-08
Contact:
MA Xiantao
E-mail:xiantaoma@126.com
Supported by:
CLC Number:
TrendMD:
YU Jing, WU Chao, LI Chenyang, CHEN Danfeng, DING Liuyue, MA Xiantao. Catalyst-free and Highly Efficient O-Silylation of Alcohols and Phenols[J]. Chem. J. Chinese Universities, 2022, 43(2): 20210588.
Compd. | 1H NMR(600 MHz, CDCl3), δ | 13C NMR(150 MHz, CDCl3), δ |
---|---|---|
3aa | 7.38—7.30(m, 4H), 7.28—7.23(m, 1H), 4.70(s, 2H), 0.16(s, 9H) | 141.0, 128.4, 127.2, 126.6, 64.7, -0.3 |
3ab | 7.25(d, J=8.4 Hz, 2H), 6.87(d, J=8.4 Hz, 2H), 4.63(s, 2H), 3.79(s, 3H), 0.15(s, 9H) | 158.9, 133.2, 128.2, 113.8, 64.5, 55.3, -0.2 |
3ac | 7.29(dd, J=8.4, 5.4 Hz, 2H), 7.10—6.92(m, 2H), 4.65(s, 2H), 0.16(s, 9H) | 162.1(d, J=244.5 Hz), 136.8(d, J=2.5 Hz), 128.3(d, J=7.6 Hz), 115.2(d, J=21.5 Hz), 64.1(s), -0.3(s) |
3ad | 7.29(d, J=8.4 Hz, 2H), 7.24(d, J=8.4 Hz, 2H), 4.64(s, 2H), 0.14(s, 9H) | 139.6, 132.8, 128.5, 127.9, 64.0, -0.3 |
3ae | 7.45(d, J=8.4 Hz, 2H), 7.20(d, J=8.4 Hz, 2H), 4.64(s, 2H), 0.16(s, 9H) | 140.2, 131.4, 128.2, 120.9, 64.0, -0.3 |
3af | 8.17(d, J=8.4 Hz, 2H), 7.47(d, J=8.4 Hz, 2H), 4.77(s, 2H), 0.17(s, 9H) | 148.8, 147.2, 126.7, 123.6, 63.6, -0.5 |
3ag | 7.45(d, J=7.2 Hz, 1H), 7.24(dd, J=7.8, 7.8 Hz, 1H), 6.98(dd, J=7.8, 7.8 Hz, 1H), 6.84(d, J=7.8 Hz, 1H), 4.74(s, 2H), 3.83(s, 3H), 0.18(s, 9H) | 156.4, 129.5, 128.0, 127.5, 120.5, 109.8, 59.8, 55.2, -0.3 |
3ah | 7.93—7.82(m, 3H), 7.80(s, 1H), 7.54—7.42(m, 3H), 4.88(s, 2H), 0.21(s, 9H) | 138.6, 133.5, 132.9, 128.1, 128.0, 127.8, 126.1, 125.7, 125.1, 125.0, 64.9, -0.2 |
3ai | 7.44(dd, J=5.4, 3.6 Hz, 2H), 7.29(dd, J=5.4, 3.6 Hz, 2H), 4.78(s, 4H), 0.19(s, 18H) | 138.1, 127.3, 127.1, 62.4, -0.3 |
3aj | 8.47(d, J=4.8 Hz, 1H), 7.68—7.64(m, 1H), 7.46(d, J=8.4 Hz, 1H), 7.12(dd, J=7.2, 5.4 Hz, 1H), 4.77(s, 2H), 0.15(s, 9H) | 161.0, 148.7, 136.7, 122.0, 120.4, 65.7, -0.5 |
3ak | 7.26—7.21(m, 1H), 6.94(dd, J=4.2, 3.0 Hz, 2H), 4.84(s, 2H), 0.15(s, 9H) | 144.6, 126.6, 125.0, 124.7, 60.0, -0.3 |
3al | 7.35—7.27(m, 2H), 7.23—7.19(m, 3H), 3.78(t, J=7.2 Hz, 2H), 2.84(t, J=7.2 Hz, 2H), 0.07(s, 9H) | 139.0, 129.2, 128.4, 126.3, 64.1, 39.6, -0.5 |
3am | 3.55(t, J=6.6 Hz, 2H), 1.56—1.45(m, 2H), 1.33—1.24(m, 4H), 0.88(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.8, 32.5, 28.1, 22.6, 14.2, -0.4 |
3an | 3.55(t, J=6.6 Hz, 2H), 1.55—1.47(m, 2H), 1.30—1.25(m, 10H), 0.86(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.9, 32.8, 31.9, 29.5, 29.4, 25.9, 22.8, 14.2, -0.4 |
3ao | 3.55(t, J=6.6 Hz, 2H), 1.53—1.47(m, 2H), 1.31—1.21(m, 14H), 0.86(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.8, 32.8, 32.0, 29.72, 29.66, 29.5, 29.4, 25.9, 22.8, 14.2, -0.4 |
3ap | 4.95(s, 1H), 4.80(s, 1H), 3.99(s, 2H), 1.70(s, 3H), 0.12 (s, 9H) | 144.5, 109.8, 66.5, 19.1, -0.4 |
3aq | 4.27(s, 2H), 0.15(d, J=4.2 Hz, 18H) | 104.2, 90.0, 51.7, -0.2 |
3ar | 7.38(d, J=7.2 Hz, 4H), 7.33(dd, J=7.2, 7.2 Hz, 4H), 7.25—7.23(m, 2H), 5.81(s, 1H), 0.12(s, 9H) | 145.0, 128.3, 127.2, 126.7, 77.3, 0.3 |
3as | 3.52(td, J=9.3, 4.3 Hz, 1H), 1.77(d, J=10.3 Hz, 2H), 1.72—1.66(m, 2H), 1.57—1.46(m, 1H), 1.29—1.19(m, 4H), 1.15—1.04(m, 1H), 0.09(s, 9H) | 71.2, 36.2, 25.6, 24.7, 0.3 |
3at | 1.46—1.20(m, 4H), 1.11(d, J=6.0 Hz, 3H), 0.88(q, J=6.0 Hz, 3H), 0.09(s, 9H). | 68.4, 41.9, 24.0, 19.3, 14.2, 0.3 |
3au | 2.08(s, 3H), 1.75(d, J=2.4 Hz, 6H), 1.61—1.53(m, 6H), 0.11(s, 9H) | 71.5, 46.1, 36.3, 31.0, 3.1 |
3av | 1.49(t, J=7.2 Hz, 3H), 1.18(s, 6H), 0.91(d, J=7.2 Hz, 2H), 0.04(s, 9H). | 71.3, 36.4, 28.7, 8.7, 2.0 |
Compd. | 1H NMR(600 MHz, CDCl3), δ | 13C NMR(150 MHz, CDCl3), δ |
3ba | 7.22(d, J=7.2 Hz, 2H), 6.96(t, J=7.2 Hz, 1H), 6.84(dd, J=9.9, 1.8 Hz, 2H), 0.26(s, 9H) | 155.24, 129.53, 121.54, 120.21, 0.32 |
3ca | 7.18(d, J=9.0 Hz, 2H), 6.76(d, J=9.0 Hz, 2H), 0.24(s, 9H) | 153.9, 129.5, 126.5, 121.5, 0.2 |
3da | 7.32(d, J=8.4 Hz, 2H), 6.71(d, J=8.4 Hz, 2H), 0.24(s, 9H). | 154.4, 132.4, 122.0, 113.9, 0.2 |
3ea | 6.76(s, 4H), 3.75(s, 3H), 0.22(s, 9H) | 154.3, 148.9, 120.8, 114.6, 55.7, 0.2 |
3fa | 7.20—7.13(m, 1H), 6.69—6.65(m, 1H), 6.63—6.61(m, 1H), 6.57—6.53(m, 1H), 0.26(s, 9H) | 163.52(d, J=245.6 Hz), 156.61(d, J=11.4 Hz), 130.12(d, J=10.1 Hz), 115.91(d, J=2.3 Hz), 108.49(d, J=21.3 Hz), 107.79(d, J=22.6 Hz), 0.23(s) |
3ga | 7.09—7.02(m, 1H), 6.97(t, J=7.3 Hz, 1H), 6.95—6.84(m, 2H), 0.26(s, 9H) | 154.34(d, J=243.8 Hz), 142.90(d, J=11.9 Hz), 124.36(d, J=3.7 Hz), 122.52(s), 122.07(d, J=6.4 Hz), 116.47(d, J=19.1 Hz), 0.17(s) |
3ha | 8.19—8.14(m, 1H), 7.86—7.79(m, 1H), 7.51—7.46(m, 3H), 7.37—7.32(m, 1H), 6.89(d, J=7.2 Hz, 1H), 0.37(s, 9H) | 151.5, 135.1, 128.0, 127.7, 126.3, 126.0, 125.2, 122.7, 121.3, 113.0, 0.5 |
3ia | 7.77(d, J=8.4 Hz, 1H), 7.73(d, J=8.4 Hz, 1H), 7.70(d, J=8.4 Hz, 1H), 7.44—7.40(m, 1H), 7.36—7.32(m, 1H), 7.21(d, J=2.4 Hz, 1H), 7.08(dd, J=8.4, 2.4 Hz, 1H), 0.32(s, 9H) | 153.1, 134.7, 129.5, 129.4, 127.7, 126.8, 126.3, 123.9, 122.2, 115.0, 0.4 |
3ja | 6.84—6.77(m, 1H), 6.77—6.67(m, 2H), 6.64—6.62(m, 1H), 3.54(b, 2H), 0.30(s, 9H) | 142.9, 138.2, 122.0, 118.6, 118.5, 115.8, 0.5 |
Table 1 1H NMR and 13C NMR data of compounds 3aa—3ja
Compd. | 1H NMR(600 MHz, CDCl3), δ | 13C NMR(150 MHz, CDCl3), δ |
---|---|---|
3aa | 7.38—7.30(m, 4H), 7.28—7.23(m, 1H), 4.70(s, 2H), 0.16(s, 9H) | 141.0, 128.4, 127.2, 126.6, 64.7, -0.3 |
3ab | 7.25(d, J=8.4 Hz, 2H), 6.87(d, J=8.4 Hz, 2H), 4.63(s, 2H), 3.79(s, 3H), 0.15(s, 9H) | 158.9, 133.2, 128.2, 113.8, 64.5, 55.3, -0.2 |
3ac | 7.29(dd, J=8.4, 5.4 Hz, 2H), 7.10—6.92(m, 2H), 4.65(s, 2H), 0.16(s, 9H) | 162.1(d, J=244.5 Hz), 136.8(d, J=2.5 Hz), 128.3(d, J=7.6 Hz), 115.2(d, J=21.5 Hz), 64.1(s), -0.3(s) |
3ad | 7.29(d, J=8.4 Hz, 2H), 7.24(d, J=8.4 Hz, 2H), 4.64(s, 2H), 0.14(s, 9H) | 139.6, 132.8, 128.5, 127.9, 64.0, -0.3 |
3ae | 7.45(d, J=8.4 Hz, 2H), 7.20(d, J=8.4 Hz, 2H), 4.64(s, 2H), 0.16(s, 9H) | 140.2, 131.4, 128.2, 120.9, 64.0, -0.3 |
3af | 8.17(d, J=8.4 Hz, 2H), 7.47(d, J=8.4 Hz, 2H), 4.77(s, 2H), 0.17(s, 9H) | 148.8, 147.2, 126.7, 123.6, 63.6, -0.5 |
3ag | 7.45(d, J=7.2 Hz, 1H), 7.24(dd, J=7.8, 7.8 Hz, 1H), 6.98(dd, J=7.8, 7.8 Hz, 1H), 6.84(d, J=7.8 Hz, 1H), 4.74(s, 2H), 3.83(s, 3H), 0.18(s, 9H) | 156.4, 129.5, 128.0, 127.5, 120.5, 109.8, 59.8, 55.2, -0.3 |
3ah | 7.93—7.82(m, 3H), 7.80(s, 1H), 7.54—7.42(m, 3H), 4.88(s, 2H), 0.21(s, 9H) | 138.6, 133.5, 132.9, 128.1, 128.0, 127.8, 126.1, 125.7, 125.1, 125.0, 64.9, -0.2 |
3ai | 7.44(dd, J=5.4, 3.6 Hz, 2H), 7.29(dd, J=5.4, 3.6 Hz, 2H), 4.78(s, 4H), 0.19(s, 18H) | 138.1, 127.3, 127.1, 62.4, -0.3 |
3aj | 8.47(d, J=4.8 Hz, 1H), 7.68—7.64(m, 1H), 7.46(d, J=8.4 Hz, 1H), 7.12(dd, J=7.2, 5.4 Hz, 1H), 4.77(s, 2H), 0.15(s, 9H) | 161.0, 148.7, 136.7, 122.0, 120.4, 65.7, -0.5 |
3ak | 7.26—7.21(m, 1H), 6.94(dd, J=4.2, 3.0 Hz, 2H), 4.84(s, 2H), 0.15(s, 9H) | 144.6, 126.6, 125.0, 124.7, 60.0, -0.3 |
3al | 7.35—7.27(m, 2H), 7.23—7.19(m, 3H), 3.78(t, J=7.2 Hz, 2H), 2.84(t, J=7.2 Hz, 2H), 0.07(s, 9H) | 139.0, 129.2, 128.4, 126.3, 64.1, 39.6, -0.5 |
3am | 3.55(t, J=6.6 Hz, 2H), 1.56—1.45(m, 2H), 1.33—1.24(m, 4H), 0.88(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.8, 32.5, 28.1, 22.6, 14.2, -0.4 |
3an | 3.55(t, J=6.6 Hz, 2H), 1.55—1.47(m, 2H), 1.30—1.25(m, 10H), 0.86(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.9, 32.8, 31.9, 29.5, 29.4, 25.9, 22.8, 14.2, -0.4 |
3ao | 3.55(t, J=6.6 Hz, 2H), 1.53—1.47(m, 2H), 1.31—1.21(m, 14H), 0.86(t, J=7.2 Hz, 3H), 0.09(s, 9H) | 62.8, 32.8, 32.0, 29.72, 29.66, 29.5, 29.4, 25.9, 22.8, 14.2, -0.4 |
3ap | 4.95(s, 1H), 4.80(s, 1H), 3.99(s, 2H), 1.70(s, 3H), 0.12 (s, 9H) | 144.5, 109.8, 66.5, 19.1, -0.4 |
3aq | 4.27(s, 2H), 0.15(d, J=4.2 Hz, 18H) | 104.2, 90.0, 51.7, -0.2 |
3ar | 7.38(d, J=7.2 Hz, 4H), 7.33(dd, J=7.2, 7.2 Hz, 4H), 7.25—7.23(m, 2H), 5.81(s, 1H), 0.12(s, 9H) | 145.0, 128.3, 127.2, 126.7, 77.3, 0.3 |
3as | 3.52(td, J=9.3, 4.3 Hz, 1H), 1.77(d, J=10.3 Hz, 2H), 1.72—1.66(m, 2H), 1.57—1.46(m, 1H), 1.29—1.19(m, 4H), 1.15—1.04(m, 1H), 0.09(s, 9H) | 71.2, 36.2, 25.6, 24.7, 0.3 |
3at | 1.46—1.20(m, 4H), 1.11(d, J=6.0 Hz, 3H), 0.88(q, J=6.0 Hz, 3H), 0.09(s, 9H). | 68.4, 41.9, 24.0, 19.3, 14.2, 0.3 |
3au | 2.08(s, 3H), 1.75(d, J=2.4 Hz, 6H), 1.61—1.53(m, 6H), 0.11(s, 9H) | 71.5, 46.1, 36.3, 31.0, 3.1 |
3av | 1.49(t, J=7.2 Hz, 3H), 1.18(s, 6H), 0.91(d, J=7.2 Hz, 2H), 0.04(s, 9H). | 71.3, 36.4, 28.7, 8.7, 2.0 |
Compd. | 1H NMR(600 MHz, CDCl3), δ | 13C NMR(150 MHz, CDCl3), δ |
3ba | 7.22(d, J=7.2 Hz, 2H), 6.96(t, J=7.2 Hz, 1H), 6.84(dd, J=9.9, 1.8 Hz, 2H), 0.26(s, 9H) | 155.24, 129.53, 121.54, 120.21, 0.32 |
3ca | 7.18(d, J=9.0 Hz, 2H), 6.76(d, J=9.0 Hz, 2H), 0.24(s, 9H) | 153.9, 129.5, 126.5, 121.5, 0.2 |
3da | 7.32(d, J=8.4 Hz, 2H), 6.71(d, J=8.4 Hz, 2H), 0.24(s, 9H). | 154.4, 132.4, 122.0, 113.9, 0.2 |
3ea | 6.76(s, 4H), 3.75(s, 3H), 0.22(s, 9H) | 154.3, 148.9, 120.8, 114.6, 55.7, 0.2 |
3fa | 7.20—7.13(m, 1H), 6.69—6.65(m, 1H), 6.63—6.61(m, 1H), 6.57—6.53(m, 1H), 0.26(s, 9H) | 163.52(d, J=245.6 Hz), 156.61(d, J=11.4 Hz), 130.12(d, J=10.1 Hz), 115.91(d, J=2.3 Hz), 108.49(d, J=21.3 Hz), 107.79(d, J=22.6 Hz), 0.23(s) |
3ga | 7.09—7.02(m, 1H), 6.97(t, J=7.3 Hz, 1H), 6.95—6.84(m, 2H), 0.26(s, 9H) | 154.34(d, J=243.8 Hz), 142.90(d, J=11.9 Hz), 124.36(d, J=3.7 Hz), 122.52(s), 122.07(d, J=6.4 Hz), 116.47(d, J=19.1 Hz), 0.17(s) |
3ha | 8.19—8.14(m, 1H), 7.86—7.79(m, 1H), 7.51—7.46(m, 3H), 7.37—7.32(m, 1H), 6.89(d, J=7.2 Hz, 1H), 0.37(s, 9H) | 151.5, 135.1, 128.0, 127.7, 126.3, 126.0, 125.2, 122.7, 121.3, 113.0, 0.5 |
3ia | 7.77(d, J=8.4 Hz, 1H), 7.73(d, J=8.4 Hz, 1H), 7.70(d, J=8.4 Hz, 1H), 7.44—7.40(m, 1H), 7.36—7.32(m, 1H), 7.21(d, J=2.4 Hz, 1H), 7.08(dd, J=8.4, 2.4 Hz, 1H), 0.32(s, 9H) | 153.1, 134.7, 129.5, 129.4, 127.7, 126.8, 126.3, 123.9, 122.2, 115.0, 0.4 |
3ja | 6.84—6.77(m, 1H), 6.77—6.67(m, 2H), 6.64—6.62(m, 1H), 3.54(b, 2H), 0.30(s, 9H) | 142.9, 138.2, 122.0, 118.6, 118.5, 115.8, 0.5 |
1 | Wang L. L., Li L., Feng S. Y., Chem. J. Chinese Universities, 2021, 42(7), 2111—2122(王琳琳, 李磊, 冯圣玉. 高等学校化学学报, 2021, 42(7), 2111—2122) |
2 | Han M. Y., Zhao L. N., Sun J., Chem. J. Chinese Universities, 2021, 42(12), 3547—3560(韩慕瑶, 赵丽娜, 孙洁. 高等学校化学学报, 2021, 42(12), 3547—3560) |
3 | De S. K., Protection and Deprotection of Common Functional GroupsAppl. Org. Chem., 2021, https://doi.org/10.1002/9783527828166.ch11 |
4 | Mittersteiner M., Voigt M. A., de Jesus P. C., Brondani P. B., Chemistry Select, 2018, 3(38), 10717—10720 |
5 | Amantini D., Fringuelli F., Pizzo F., Vaccaro L., J. Org. Chem., 2001, 66(20), 6734—6737 |
6 | Field L. D., Messerle B. A., Rehr M., Soler L. P., Hambley T. W., Organometallics, 2003,22(12), 2387—2395 |
7 | Blandez J. F., Primo A., Asiri A. M., Álvaro M., García H., Angew. Chem. Int. Ed., 2014, 53(46), 12581—12586 |
8 | Chen B. F., Li F. B., Mei Q. Q., Yang Y. D., Liu H. Z., Yuan G. Q., Han B. X., Chem. Commun., 2017, 53(97), 13019—13022 |
9 | Park J. W., Jun C. H., Org. Lett., 2007, 9(20), 4073—4076 |
10 | Hreczycho G., Chmielewski M. K., Maciejewski H., Ratajczak T., Marciniec B., Tetrahedron Lett., 2013, 54(28), 3605—3608 |
11 | Kuciński K., Stachowiak H., Hreczycho G., Eur. J. Org. Chem., 2020, 2020(26), 4042—4049 |
12 | Aghapour G., Moghaddam A. K., Nadali S., J. Chin. Chem. Soc., 2015, 62(2), 197—203 |
13 | Park J. W., Jun C. H., Org. Lett., 2007, 9(20), 4073—4076 |
14 | Karimi B., Golshani B., J. Org. Chem., 2000, 65(21), 7228—7230 |
15 | Jin T. S., Tian R. F., Liu L. B., Zhao Y., Li T. S., Synth. Commun., 2006, 36(13), 1823—1828 |
16 | Shirini F., Khoshdel M. A., Abedini M., Atghia S. V., Chin. Chem. Lett., 2011, 22(10), 1211—1214 |
17 | Dhakshinamoorthy A., Santiago⁃Portillo A., Concepción P., Herance J. R., Navalón S., Alvaro M., Garcia H., Catal. Sci. Technol., 2017, 7(12), 2445—2449 |
18 | Pantawane A. R., Thul M., Lin Y. J., Lin M., Lin W., Julakanti S. R., Wu H. R., Luo S. Y., Catalysts, 2021, 11(7), 825 |
19 | Kadam S. T., Kim S. S., Green Chem., 2010, 12(1), 94—98 |
20 | Ma X. T., Yu J., Han C. J., Zhou Q. J., Ren M. J., Li L. X., Tang L., Adv. Synth. Catal.,2019, 361(5),1023—1027 |
21 | Ma X. T., Yu J., Zhou Q. J., Yan R., Zheng L. Y., Wang L. L., J. Org. Chem., 2019, 84(11), 7468—7473 |
22 | Ma X. T., Yu J., Ma R. T., Yan R., Zhang Z. L., Chin. J. Org. Chem., 2019, 39(3), 830—835(马献涛, 于静, 马瑞甜, 燕然, 张振雷. 有机化学, 2019, 39(3), 830—835) |
23 | Zhou Q. J., Zheng L. Y., Ma B., Huang L. J., Liu A. Q., Cao X. H., Yu J., Ma X. T., J. Org. Chem., 2020, 85(7), 5097—5103 |
24 | Yu J., Chang X. P., Ma R. T., Zhou Q. J., Wei M. M., Cao X. H., Ma X. T., Eur. J. Org. Chem.,2020, 2020(46), 7238—7242 |
25 | Ma X. T., Yu J., Wang Z. L., Zhang Y., Zhou Q. J., Chin. J. Org. Chem., 2020, 40(9), 2669—2677(马献涛, 于静, 王子龙, 张赟, 周秋菊. 有机化学, 2020, 40(9), 2669—2677) |
26 | Ma X. T., Yu J., Jiang M. Y., Wang M. Y., Tang L., Wei M. M., Zhou Q. J., Eur. J. Org. Chem., 2019, 2019(28), 4593—4596 |
27 | Ma X. T., Zhou K. J., Ren M. J., Wang M. Y., Yu J., Chin. J. Org. Chem., 2019, 39(10), 2796—2801(马献涛, 周坤洁, 任梦娟, 王梦雨, 于静. 有机化学, 2019, 39(10), 2796—2801) |
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