Sulfuric Acid → D-Altrose
反応式
[C@@H:1]12[O:11][CH2:10][C@@H:8]([O:9]1)[C@@H:6]([OH:7])[C@@H:4]([OH:5])[C@@H:2]2[OH:3].S(=O)(=O)(O)[OH:13]>>[O:13]=[CH:10][C@H:8]([C@@H:6]([C@@H:4]([C@@H:2]([CH2:1][OH:11])[OH:3])[OH:5])[OH:7])[OH:9]参加物
3
実験手順
0.16 g (1.00 mmol) of the compound (3) was dissolved in 5 ml of 1N sulfuric acid, and the resultant solution was kept stirred for 5 hours at 100° C. The reaction mixture was passed through an anion exchange resin (hydroxyl ion type amberlight IRA-410) for neutralizing purposes, followed by removing the solvent by means of distillation under reduced pressure. Formation of the desired compound of the present invention, i.e., D-altrose (compound 4), was confirmed by thin layer chromatography. It was also confirmed that the raw material compound (3) was mixed with the product compound (4). The mixing ratio of these compounds (3) and (4) was about 1:1.
後処理
- customby removing the solvent
- distillationby means of distillation under reduced pressure
- additionwas mixed with the product compound (4)
出典と根拠
- ORDレコード
- ord-b2d3430ac16242b983ab593c14c129e6
- 出典データセット
- uspto-grants-1995_04
- 特許番号
- US05410038
反応ノート
読み込み中…