反応式
O=[Cr](=O)=O.C1C=CC=CN=1.C1C=CC=CN=1.[CH3:17][O:18][C:19](=[O:41])[CH2:20][CH2:21][CH2:22]/[CH:23]=[CH:24]\[CH2:25][C@H:26]1[C@H:30]([Cl:31])[CH2:29][C@@H:28]([O:32][CH:33]2[CH2:38][CH2:37][CH2:36][CH2:35][O:34]2)[C@@H:27]1[CH2:39][OH:40].C(=O)(O)[O-].[Na+].S(=O)(=O)(O)O>ClCCl.C(OCC)C.O>[CH3:17][O:18][C:19](=[O:41])[CH2:20][CH2:21][CH2:22]/[CH:23]=[CH:24]\[CH2:25][C@H:26]1[C@H:30]([Cl:31])[CH2:29][C@@H:28]([O:32][CH:33]2[CH2:38][CH2:37][CH2:36][CH2:35][O:34]2)[C@@H:27]1[CH:39]=[O:40]参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
9 g of Collins reagent is dissolved in 85 ml of dichloromethane, and a solution of 2 g of VI in 25 ml of dichloromethane is instilled with stirring in 5 minutes, stirred 15 minutes, diluted with 200 ml of diethyl ether, shaken with sodium bicarbonate solution, diluted sulfuric acid and salt water, dried over magnesium sulfate and concentrated by evaporation in a vacuum. 1.72 g of aldehyde VII is obtained as oil.
後処理
- stirringstirred 15 minutes
- dry with materialdried over magnesium sulfate
- concentrationconcentrated by evaporation in a vacuum
出典と根拠
- ORDレコード
- ord-051427dba65341b6baa3b71a29f94bfe
- 出典データセット
- uspto-grants-1989_02
- 特許番号
- US04806668
関連ノート
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