Hydroxy Functionalized Tertiary Phosphines

References

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• Satisfactory analyses for C and H were obtained for all these compounds. NMR(CDC13, TMS) data, in δ ppm, are as follows: 1 1.97(d,6H, J=13Hz,2CH3), 3.38(s,3H, O.CH3), 4.48(s,2H, CH2), 7.62(m,4H, C6H4); 2 1.06(m,3H, CH3), 1.82(d,3H, J=13Hz, CH3), 2.10(m,2H, CH2), 3.38(s,3H, OCH3), 4.48(s,2H, CH2), 7.64(m,4H, C6H4); 3 1.17(m,3H, CH3), 2.13(m,2H, CH2), 3.42(s,3H, OCH3), 4.47 (s,2H, CH2), 7.57(m,4H, C6H4); 4 1.96(d,6H, J=13Hz,2CH3), 2.92 (t,2H, CH2), 3.33(s,3H, OCH3), 3.63(t,2H, CH2), 7.63(m,4H, C6H4); 5 1.05(m,3H, CH3), 2.03(m,2H, CH2), 2.83(t,2H, CH2), 3.26(s,3H, OCH3), 3.54(t,2H, CH2), 7.54(m,4H, C6H4); 6 2.00(d,6H, J=13Hz, 2CH3), 2.78(s,1H, OH), 4.68(s,2H, CH2), 7.66(m,4H, C6H4); 7 2.06 (m,3H, CH3), 2.18(m,2H, CH2), 2.80(s,1H, OH), 4.66(s,2H, CH2), 7.60 (m,4H, C6H4); 8 1.06(m,3H, CH3), 1.95(t,2H, CH2), 2.05(t,2H, CH2), 2.86(t,2H, CH2), 3.81(t,2H, CH2), 7.52(m,4H, C6H4); 9 2.01 (d,6H, J=13Hz,2CH3), 2.16(s,3H, OAc), 5.15(s,2H, CH2), 7.73(m,4H, C6H4); 10 1.06(m,3H, CH3), 2.06(m,2H, CH2), 2.16(s, 3H, OAc), 5.13(s,2H, CH2), 7.66(m,4H, C6H4)
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• All these compounds are liquids, and showed satisfactory analyses for C and H. NMR(CDC13, TMS) data in δ ppm are as follows: 11 (bp. 66–8/0.2mmHg) 1.31(d,6H, J=3Hz,2CH3), 3.32(s, 3H, OCH3), 4.37(s,2H, CH2), 7.32(m,4H, C6H4); 12 1.00(m,3H, CH3), 1.30(d,3H, J=3Hz, CH3), 1.55(m,2H, CH2), 3.36(s,3H, OCH3), 4.41(s, 2H, CH2), 7.42(m,4H, C6H4); 13 (bp.80/0.3mmHg) 1.05(m,3H, CH3), 1.67(m,2H, CH2), 3.37 (s,3H, OCH3), 4.45(s,2H, CH2), 7.42(m,4H, C6H4); 14 1.30(d,6H, J=3Hz,2CH3), 2.84(t,2H, CH2), 3.36(m,3H, OCH3), 3.36(t,2H, CH2), 7.33(m,4H, C6H4); 15 1.00(m, 3H, CH3), 1.71(m,2H, CH2), 2.90(t,2H, CH2), 3.36(s,3H, OCH3), 3.63(t,2H, CH2), 7.37(m,4H, C6H4); 16 1.32(d,6H, J=3Hz,2CH3), 2.38(s, lH, OH), 4.63(s,2H, CH2), 7.28(m,4H, C6H4); 17 0.92(m,3H, CH3), 1.66 (m,2H, CH2), 2.62(s,1H, OH), 4.66(s,2H, CH2), 7.38(m,4H, C6H4); 18 1.05(m,3H, CH3), 1.73(m,2H, CH2), 2.60(s,1H, OH), 2.85(t,2H, CH2), 3.85(t,2H, CH2), 7.45(m,4H, C6H4); 19 1.30(d,6H, J=3Hz,2CH3), 2.33(s,3H, CH3), 7.17(m,4H, C6H4); 20 0.90(m,3H, CH3), 1.25(d,3H, J-3Hz, CH3), 1.60(m,2H, CH2), 2.30(s,3H, CH3), 7.26(m,4H, C6H4); 21 1.02(m,3H, CH3), 1.67(m,2H, CH2), 2.33(s,3H, CH3), 7.18(m,4H, C6H4)
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