9,12,15-cis-Octadecatrienoic acid → N-(cis-9,12,15-octadecatrienoyl)-O-phospho-2-aminoethanol
Reaktionsgleichung
[C:1]([NH:22][CH2:23][CH2:24][O:25][P:26](=[O:28])=[O:27])(=[O:21])[CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7][CH:8]=[CH:9][CH2:10][CH:11]=[CH:12][CH2:13][CH:14]=[CH:15][CH2:16][CH2:17][CH2:18]CC.C(O)(=O)CCCCCCC/C=C\CC=CCC=CCC>>[C:1]([NH:22][CH2:23][CH2:24][O:25][P:26](=[O:28])=[O:27])(=[O:21])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH:12]=[CH:13][CH2:14][CH:15]=[CH:16][CH2:17][CH3:18]Komponenten
3
Versuchsvorschrift
This compound was prepared as described above for (5), using 0.5 mmol (139 mg) of cis-9,12,15-octadecatrienoic acid; yield 80 mg, (40%); Rf 0.10-0.15 (system B); 1H-NMR (CD3SOCD3, 200 MHz) δ0.9-1.0 (t, 8H, ω-CH3); 1.3(s, 8H, 4CH2); 1.4-1.5(br, s, 2H, CH2CH2CO); 2.0-2.2 (m, 6H, CH2CO and 2CH2CH═CH); 2.7-2.9 (br s, 4H, 2HC═CH—CH2—CH═CH); 3.1-3.2 (br s, 2H, CH2NH); 3.7-3.8 (br s, 2H, CH2OP); 5.2-5.4 (br s, 6H, 3HC═CH); 8.2-8.4 (m, 3H, NH and 2POH).
Aufarbeitung
- customThis compound was prepared