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MS-NW-5450 (1-ethyl-2-pyrrolidinyl)methanol C7H15NO (Mass of molecular ion: 129)
Source Temperature: 260 °C Sample Temperature: 190 °C Reservoir, 75 eV
15.0 1.6 17.0 1.8 18.0 7.7 26.0 1.0 27.0 6.3 28.0 14.0 29.0 6.2 30.0 3.8 31.0 2.4 39.0 3.6 41.0 9.2 42.0 6.3 43.0 7.1 44.0 4.0 53.0 1.4 54.0 2.7 55.0 4.2 56.0 5.2 57.0 1.7 58.0 2.7 67.0 1.6 68.0 5.9 69.0 2.1 70.0 26.0 71.0 2.5 80.0 1.3 82.0 3.1 83.0 1.2 84.0 1.6 96.0 6.6 97.0 2.0 98.0 100.0 99.0 7.3 110.0 1.4 111.0 2.2 114.0 1.9 128.0 1.5
400 MHz in CDCl3
90 MHz in CDCl3
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1H NMR 399.65 MHz C7 H15 N O 0.05 ml : 0.5 ml CDCl3 (1-ethyl-2-pyrrolidinyl)methanol Assign. Shift(ppm)
A 3.7 B *1 3.594 C *1 3.439 D *2 3.17 E *3 2.839 F 2.554 G *3 2.283 J *2 2.214 K 1.88 L 1.78 to 1.69 M 1.105 ASSIGNED BY H-H COSY. J(B,C)=-10.8HZ. J(B,F)=4.2HZ. J(C,F)=3.1HZ. J(E,G)=-12.0HZ. J(E,M)=7.4HZ. J(G,M)=7.1HZ.
Hz ppm Int.
1447.27 3.622 41 1444.46 3.615 185 1440.31 3.604 189 1436.28 3.594 41 1433.72 3.588 240 1429.44 3.577 238 1380.49 3.455 223 1377.44 3.447 224 1369.75 3.428 166 1366.58 3.420 166 1275.39 3.192 62 1274.17 3.189 48 1271.12 3.181 90 1269.41 3.177 79 1265.99 3.168 100 1261.47 3.157 91 1257.93 3.148 52 1256.47 3.144 52 1152.34 2.884 42 1144.90 2.865 122 1140.38 2.854 55 1137.57 2.847 128 1132.93 2.835 138 1130.13 2.828 53 1125.49 2.817 135 1118.16 2.798 47 1032.10 2.583 34 1027.95 2.573 60 1026.73 2.570 62 1023.56 2.562 94 1019.29 2.551 88 1017.70 2.547 66 1016.24 2.543 63 1014.53 2.539 63 1010.38 2.529 46 929.20 2.326 56 922.12 2.308 162 917.11 2.295 63 915.04 2.290 173 910.03 2.278 152 907.96 2.272 71 903.08 2.260 155 897.46 2.246 85 896.00 2.242 73 888.43 2.224 165 883.79 2.212 41 880.86 2.205 103 880.00 2.202 135 875.00 2.190 31 871.70 2.182 65 762.70 1.909 50 760.74 1.904 30 758.67 1.899 67 753.91 1.887 83 751.22 1.880 57 749.76 1.877 98 745.24 1.865 73 742.92 1.859 63 740.84 1.854 62 736.69 1.844 36 717.90 1.797 35 717.29 1.795 37 712.28 1.783 79 711.18 1.780 59 708.98 1.775 60 706.54 1.768 81 705.69 1.766 79 704.22 1.763 101 703.13 1.760 105 701.42 1.756 76 699.46 1.751 215 696.29 1.743 197 694.21 1.738 296 692.50 1.733 186 689.82 1.727 255 686.52 1.718 134 685.91 1.717 132 681.40 1.705 125 678.47 1.698 52 677.37 1.695 47 672.97 1.684 37 448.97 1.124 646 441.65 1.106 1000 434.45 1.088 634
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1H NMR 89.56 MHz C7 H15 N O 0.04 ml : 0.5 ml CDCl3 (1-ethyl-2-pyrrolidinyl)methanol Assign. Shift(ppm)
A *1 3.603 B *1 3.389 C *2 3.17 D *2 2.90 to 2.51 E *2 2.34 to 2.12 F 1.95 to 1.67 G 1.102
Hz ppm Int.
332.31 3.711 111 328.44 3.668 119 321.63 3.592 265 317.88 3.550 301 309.19 3.453 218 306.63 3.424 245 298.56 3.334 94 295.88 3.304 105 293.31 3.276 62 288.94 3.227 74 288.75 3.225 74 288.25 3.219 64 287.94 3.216 60 285.31 3.186 48 284.13 3.173 81 281.00 3.138 63 280.56 3.133 65 280.06 3.128 69 279.31 3.119 69 278.94 3.115 63 262.06 2.927 90 257.56 2.876 61 254.75 2.845 108 252.88 2.824 51 252.38 2.818 48 251.94 2.814 48 250.13 2.793 167 248.81 2.779 83 247.50 2.764 110 246.19 2.749 91 245.88 2.746 93 245.44 2.741 90 245.06 2.737 85 244.31 2.728 91 242.81 2.712 193 241.00 2.691 87 240.00 2.680 70 238.94 2.668 66 238.44 2.663 66 238.13 2.659 70 237.63 2.654 66 235.50 2.630 117 233.31 2.606 69 232.88 2.601 65 232.25 2.594 71 231.81 2.589 78 231.13 2.581 83 230.31 2.572 71 229.94 2.568 69 228.94 2.557 62 228.44 2.551 65 227.94 2.546 68 227.56 2.541 66 226.50 2.530 59 225.75 2.521 48 224.25 2.504 50 223.75 2.499 54 223.25 2.493 49 220.94 2.467 84 213.75 2.387 174 212.56 2.374 49 209.00 2.334 61 206.81 2.310 175 205.38 2.294 48 204.38 2.283 111 203.19 2.269 64 202.44 2.261 79 201.81 2.254 125 200.00 2.234 103 197.13 2.202 97 194.81 2.176 144 188.06 2.100 107 173.63 1.939 58 171.50 1.915 52 168.94 1.887 54 168.56 1.883 53 164.88 1.842 139 163.56 1.827 191 162.63 1.816 118 161.31 1.802 223 160.81 1.796 212 160.06 1.788 285 158.31 1.768 260 157.19 1.756 243 156.13 1.744 275 154.94 1.731 162 153.94 1.719 147 152.88 1.708 125 152.13 1.699 141 151.81 1.696 135 151.50 1.692 135 149.50 1.670 82 147.94 1.652 69 147.13 1.643 49 145.50 1.625 48 105.63 1.180 525 98.25 1.098 1000 91.25 1.019 404
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