L-Gulose → Anhydro-d-mannosan
反応式
O=[CH:2][C@H:3]([C@H:5]([C@@H:7]([C@H:9]([CH2:11][OH:12])[OH:10])[OH:8])[OH:6])[OH:4]>O>[C@@H:11]12[O:12][CH2:2][C@H:3]([O:4]1)[C@@H:5]([OH:6])[C@H:7]([OH:8])[C@@H:9]2[OH:10]参加物
3
試薬・触媒・溶媒 1
実験手順
Syrupy L-gulose was heated on a steam bath in water with strong acid resin (Dowex 50 W-X8, H+ form) for 64 h. The solution was then filtered, the resin washed with water, and the combined filtrate was passed onto a column packed with strong base resin (Amberlite IRA-900, OH- form). The column was washed with distilled water to elute the title compound which crystallized from ethanol. Recrystallized from ethanol it has mp 155.5°-156.5° C. The column was then immediately washed with aqueous acetic acid (M) to elute unreacted L-gulose which was recycled to provide further title compound.
後処理
- filtrationThe solution was then filtered
- washthe resin washed with water
- washThe column was washed with distilled water
- washto elute the title compound which
- customcrystallized from ethanol
- customRecrystallized from ethanol it
- washThe column was then immediately washed with aqueous acetic acid (M)
- washto elute unreacted L-gulose which
出典と根拠
- ORDレコード
- ord-7071e9fa7c1e442a8c0394816aa747f6
- 出典データセット
- uspto-grants-1991_09
- 特許番号
- US05047518
反応ノート
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