Acetic Anhydride → L-Galactose, 6-deoxy-, 2,3,4,5-tetraacetate
反応式
[O:1]=[CH:2][C@H:3]([C@@H:5]([C@@H:7]([C@H:9]([CH3:11])[OH:10])[OH:8])[OH:6])[OH:4].C(O[C:16](=[O:18])[CH3:17])(=O)C>N1C=CC=CC=1>[C:2]([O:4][C@@H:3]([C@@H:5]([C@@H:7]([C@H:9]([CH3:11])[O:10][C:16](=[O:18])[CH3:17])[O:8][C:9](=[O:10])[CH3:11])[O:6][C:5](=[O:6])[CH3:7])[CH:2]=[O:1])(=[O:1])[CH3:3]参加物
4
実験手順
To a solution of L-fucose (1.03 g, 6.09 mmol) in 60 mL of pyridine at room temperature is added acetic anhydride (4.6 mL, 4.96 g, 48.7 mmol). The solution is stirred at room temperature for 20 h and concentrated in vacuo. The residue is then dissolved in 50 mL of CH2Cl2 and washed with 5% HCl (4×60 mL), dried over anhydrous Na2SO4 and concentrated to afford 1.76 g (85%) of L-fucose tetraacetate 1 as a white foam, a 5:2 (α:β) mixture of anomers: Rf 0.38 (40% petroleum ether/EtOAc); 1H NMR (CDCl3, 270 MHz, mixture of anomers) δ 6.33 (d, J=2.0 Hz, 1H, H-1α), 5.67 (d, J=8.2 Hz, 1H, H-1β), 5.26-5.38 (m, 5H), 5.06 (dd, J=10.4, 3.4 Hz, 1H, H-3b), 4.27 (q, J=6.6 Hz, 1H, H-5α), 3.95 (q, J=6.3 Hz, 1H, H-5β), 2.23 (s, 3H), 2.19 (s, 3H), 2.18 (s, 3H), 2.17 (s, 3H), 2.15 (s, 3H), 2.04 (s, 3H), 2.02 (s, 3H), 2.01 (s, 3H), 1.22 (d, J=6.6 Hz, 3H, H-6β), 1.16 (d, J=6.6 Hz, 3H, H-6α).