SYNTHESIS OF GLYCIDYL PROPARGYL ETHER
1741
3
3
3
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4.9 Hz), 3.16 d.d.d.d (1H, ОCH2СН, J 5.9, J 4.9, J
3
2
3
3.1, J 2.6 Hz), 3.48 d.d (1H, ОCH2СН, J 11.4, J
2
3
5.9 Hz), 3.81 d.d (1H, ОCH2СН, J 11.4, J 3.8 Hz),
4.19 d, 4.22 d (2HАВ, ОCH2С≡, 2J 15.6, 4J 2.4 Hz). 13C
NMR spectrum, δ, ppm: 44.00 (ОCH2, cycle), 50.24
(ОCH2СН), 58.20 (ОCH2С≡), 70.15 (ОCH2СН), 74.67
(НС≡), 79.15 (C≡). Signals assignment in the 13С
NMR spectrum was done with the help of 2D
correlation HSQC. Found, %: С 64.41; H 7.10.
C6H8О2. Calculated, %: C 64.27; H 7.19.
NMR spectra were registered on a spectrometer
Bruker DPX-400 [400.13 (1Н) and 100.62 (13С) МHz];
heteronuclear correlation experiment 1Н–13С HSQC was
carried out on an instrument Bruker AV-400 in CDCl3;
internal references HMDS (δH 0.05 ppm), CDCl3 (δC
77.00 ppm). IR spectrum was recorded on a spectro-
photometer Varian 3100 FT-IR. All reagents and
solvents used in the study were commercial products.
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Gakhramanov, R.F., Izv. Vuzov, Ser. Khim. Khim.
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ACKNOWLEDGMENTS
The study was carried out using the equipment of
Baikal analytic center of joint usage of Siberian
Department of the Russian Academy of Sciences.
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Liu, R.-S., J. Am. Chem. Soc., 2001, vol. 123, p. 7427.
doi 10.1021/ja0106016
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RUSSIAN JOURNAL OF ORGANIC CHEMISTRY Vol. 53 No. 11 2017