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nin, A.B., Mironova, E.V., Krivolapov, D.B., Buzy-
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1134, 1090, 1057, 1003, 967, 909, 869, 771, 666, 640,
1
559, 484, 426, 405. H NMR spectrum, δ, ppm: 0.89 t
3
(6H, CH2CH3, JHN = 7.3 Hz), 1.34 s (6H, 4-H), 1.36–
1.43 m (4H, CH2CH3), 1.46–1.62 m (4H, PCH2CH2),
3
1.64–1.83 m (4H, PCH2), 5.33 d.d (1H, 2-H, JPH
=
=
3
2
24.2, JHH = 14.1 Hz), 6.67 d.d (1H, 1-H, JPH
37.3, JHH = 14.1 Hz). 31P–{1H} NMR spectrum:
3
δP 43.5 ppm. Mass spectrum: m/z 285 [M + K]+·.
(Z)-(4-Diphenylphosphoryl)-2-methylbut-3-en-1-
ol (4e). Yield 4.3 g 84%), white powder, mp 100–
102°C; published data [28, 29]: mp 103–104°C.
IR spectrum, ν, cm–1: 3257, 3077, 3057, 2975, 2926,
1619, 1591, 1484, 1462, 1437, 1355, 1271, 1163,
1138, 1118, 1096, 1070, 1028, 998, 966, 756, 732, 715,
1
691, 658, 561, 521, 475, 422. H NMR spectrum, δ,
ppm: 1.45 s (6H, 4-H), 5.95 d.d (1H, 2-H, 3JPH = 24.2,
3JHH = 14.0 Hz), 6.87 d.d (1H, 1-H, 2JPH = 40.3, 3JHH
=
14.0 Hz), 7.46 m (4H, m-H), 7.52 m (2H, p-H), 7.72 m
(4H, o-H). 31P–{1H} NMR spectrum: δP 26.7 ppm.
This study was performed under financial support
by the Russian Foundation for Basic Research (project
no. 14-33-50701_mol_nr).
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