Acetic Acid → 2,3,6,3',4'-penta-O-acetylsucrose

HRID 1902357ノート

反応式

HRID 1902357 の反応式
CC([O:4][C@@H:5]1[C@H:10]([O:11][C:12]([CH3:14])=[O:13])[C@@H:9]([O:15][C:16]([CH3:18])=[O:17])[C@@H:8]([O:19][C@:20]2([CH2:35][OH:36])[O:24][C@H:23]([CH2:25][OH:26])[C@@H:22]([O:27][C:28]([CH3:30])=[O:29])[C@@H:21]2[O:31][C:32]([CH3:34])=[O:33])[O:7][C@@H:6]1[CH2:37]O)=O.[C:39]([OH:42])(=[O:41])[CH3:40]>C(C(C)=O)C(C)C>[CH3:40][C:39]([O:42][CH2:37][C@H:6]1[O:7][C@H:8]([O:19][C@@:20]2([CH2:35][OH:36])[O:24][C@@H:23]([CH2:25][OH:26])[C@@H:22]([O:27][C:28]([CH3:30])=[O:29])[C@H:21]2[O:31][C:32]([CH3:34])=[O:33])[C@H:9]([O:15][C:16]([CH3:18])=[O:17])[C@@H:10]([O:11][C:12]([CH3:14])=[O:13])[C@@H:5]1[OH:4])=[O:41]

参加物

4

実験手順

2,3,4,3',4'-penta-O-acetyl sucrose (2 g) was dissolved in methyl isobutyl ketone (20 ml) and acetic acid (1 ml) was added. The reaction of the mixture was heated under reflux (about 126°) for 3 hours. On cooling, the product crystallized to give a yield of 1.5 g (75%) of 2,3,6,3',4'-penta-O-acetyl sucrose.

後処理

  1. customThe reaction of the mixture
  2. temperaturewas heated
  3. temperatureunder reflux (about 126°) for 3 hours
  4. temperatureOn cooling
  5. customthe product crystallized

出典と根拠

ORDレコード
ord-13b74101cd8d4b0d9406b7bfb7d80f40
出典データセット
uspto-grants-1982_12
特許番号
US04362869

反応ノート

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