反応式
[CH3:1][C@@H:2]([C@@H:8]1[C@@:12]2([CH3:29])[C@@H:13]([OH:28])[CH2:14][C@@H:15]3[C@@:20]4([CH3:26])[CH2:21][CH2:22][C@@H:23]([OH:25])[CH2:24][C@H:19]4[CH2:18][C@@H:17]([OH:27])[C@H:16]3[C@@H:11]2[CH2:10][CH2:9]1)[CH2:3][CH2:4][C:5]([OH:7])=[O:6].[S:30](Cl)([CH3:33])(=[O:32])=[O:31].OS(O)(=O)=O.CC(=O)OCC>N1C=CC=CC=1.O.C(O)(=O)C>[OH:27][CH:17]1[CH:16]2[CH:15]([CH2:14][CH:13]([OH:28])[C:12]3([CH3:29])[CH:11]2[CH2:10][CH2:9][CH:8]3[CH:2]([CH3:1])[CH2:3][CH2:4][C:5]([OH:7])=[O:6])[C:20]2([CH3:26])[CH:19]([CH2:24][CH:23]([O:25][S:30]([CH3:33])(=[O:32])=[O:31])[CH2:22][CH2:21]2)[CH2:18]1参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
100 g of cholic acid are dissolved in 500 ml of pyridine and 23.1 ml of mesyl chloride are added dropwise at 0° C. over a period of 30 minutes. The mixture is stirred at RT for 3 hours, then poured onto a solution of 400 ml of H2SO4 in 3 l of water at 0° C. and extracted 4 times with 750 ml of EA each time. The organic phase is dried over Na2SO4 and the solvent is removed in vacuo. The residue is crystallized using diisopropyl ether and 117.1 g are obtained; m.p. 121° C. (with decomposition). Rf (EA/HEP/acetic acid 5:5:1)=0.31 MS (FAB): 487 (M+H)+
後処理
- extractionextracted 4 times with 750 ml of EA each time
- dry with materialThe organic phase is dried over Na2SO4
- customthe solvent is removed in vacuo
- customThe residue is crystallized
- customare obtained
出典と根拠
- ORDレコード
- ord-4bb7fd5933aa45639c928c5bb31f2603
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06166002
関連ノート
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