Ethanol → (S)-((3R,3aR,6R,6aR)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl) 5,6-bis(nitrooxy)hexanoate
反応式
[N+:1]([O:4][C@H:5]([CH2:27][O:28][N+:29]([O-:31])=[O:30])[CH2:6][CH2:7][CH2:8][C:9]([O:11][C@@H:12]1[CH2:16][O:15][C@@H:14]2[C@H:17]([O:20]C3CCCCO3)[CH2:18][O:19][C@H:13]12)=[O:10])([O-:3])=[O:2].C(O)C>>[N+:1]([O:4][C@H:5]([CH2:27][O:28][N+:29]([O-:31])=[O:30])[CH2:6][CH2:7][CH2:8][C:9]([O:11][C@@H:12]1[CH2:16][O:15][C@@H:14]2[C@H:17]([OH:20])[CH2:18][O:19][C@H:13]12)=[O:10])([O-:3])=[O:2]参加物
3
反応条件
- 温度
- 45 °C
実験手順
To a solution of (5S)-((3R,3aR,6R,6aR)-6-(tetrahydro-2H-pyran-2-yloxy)hexahydrofuro[3,2-b]furan-3-yl) 5,6-bis(nitrooxy)hexanoate (2.27 g, 5.04 mmol) in ethanol (40 mL) pyridinium p-toluensulfonate (127 mg, 0.504 mmol) was added The reaction mixture was stirred at 45° C. for 4 hrs. The reaction mixture was filtered, concentrated under reduced pressure. The crude residue was purified by flash chromatography (Biotage SP1, EtOAc/n-hexane from 10 to 60%), affording the title product as pale yellow oil.