Diethyl Ether → 8-Pentadecanyl 2,3,4,6-tetra-O-acetyl-D-glucopyranoside
反応式
[C:1]([O:4]O)(=[O:3])[CH3:2].[O:6]=[CH:7][C@@H:8]([C@H:10]([C@@H:12]([C@@H:14]([CH2:16][OH:17])O)[OH:13])[OH:11])[OH:9].[CH3:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH:25](O)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].B(F)(F)F.[O:38]([CH2:41][CH3:42])CC>ClCCCl>[C:1]([O:4][C@@H:14]1[C@@H:12]([O:13][C:1](=[O:3])[CH3:2])[C@H:10]([O:11][C:7](=[O:6])[CH3:8])[C@@H:8]([CH2:7][O:6][C:41](=[O:38])[CH3:42])[O:9][CH:16]1[O:17][CH:25]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH3:18])(=[O:3])[CH3:2]参加物
実験手順
To a solution of D-glucose peracetate (250 mg, 640 μmol) in DCE (1 mL) was added 8-pentadecanol (220 mg, 960 μmol). BF3.O(Et)2 (134 μL, 1.1 mmol) was added and the mixture stirred at room temperature overnight before pouring onto short plug of silica and eluting with EtOAc. The solvent was evaporated before the crude material was purified by column chromatography (SiO2, loaded with DCM, elution with DCM (100 mL), then 20% EtOAc/Hexane to 35% EtOAc/Hexane) to give the glycoside 141 as a white solid (179 mg, 50%). 1H NMR (CDCl3, 400 MHz) δ: 5.19 (dd, 1H, J2,3=9.5, J3,4=0.0, H-3), 5.06 (dd, 1H, J4,5=9.7, H-4), 4.96 (dd, 1H, J1,2=8.0, J2,3=9.6, H-2), 4.52 (d, 1H, H-1), 4.21 (dd, 1H, J5,6b=5.2, J6a,6b=12.1, H-6b), 4.12 (dd, 1H, J5,6a=2.6, H-6a), 3.66 (ddd, 1H, J4,5=10.0, H-5), 3.53 (m, 1H, CH2CHOCH2), 2.07 (s, 3H, OCOCH3), 2.02 (s, 6H, OCOCH3), 2.00 (s, 3H, OCOCH3), 1.60-1.20 (m, ˜24H, CH2), 0.88 (t, 3H, J=7.0, CH3), 0.87 (t, 31-1, J=7.0, CH3).
後処理
- additionbefore pouring onto short plug of silica
- washeluting with EtOAc
- customThe solvent was evaporated before the crude material
- customwas purified by column chromatography (SiO2
- washloaded with DCM, elution with DCM (100 mL)
出典と根拠
- ORDレコード
- ord-fbbd812579b9474eab3576fa1ed53879
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08828952B2
反応ノート
読み込み中…