反応式
[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH:22]([CH3:24])[CH3:23])=[CH:6][CH:7]=[C:8]([CH3:21])[CH2:9][CH2:10][CH:11]=[C:12]([CH3:20])[CH2:13][CH2:14][CH:15]=[C:16]([CH3:19])[CH2:17]O)[CH3:2].CC1C=C(C)N=C(C)C=1.[Cl-].[Li+].CS([Cl:41])(=O)=O>C(OCC)C.O.CN(C)C=O>[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH:22]([CH3:24])[CH3:23])=[CH:6][CH:7]=[C:8]([CH3:21])[CH2:9][CH2:10][CH:11]=[C:12]([CH3:20])[CH2:13][CH2:14][CH:15]=[C:16]([CH3:19])[CH2:17][Cl:41])[CH3:2]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
To a mixture of the hydroxyester compound which is 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoic acid ethyl ester (71.0 mg, 0.20 mmol), S-collidine (26.7 mg, 0.22 mmol), lithium chloride (8.5 mg, 0.20 mmol) and dimethylformamide (1 ml) is added methanesulfonyl chloride (25.2 mg, 0.22 mmol) under nitrogen atmosphere while stirring on an ice-bath. The stirring is continued at the same temperature for 5 hours. After confirming disappearance of the starting compound, to the reaction mixture are added water and ethyl ether and the organic layer is separated. The organic layer is washed with water, dried (MgSO4) and concentrated. The resulting residue is chromatographed (n-hexane/ethyl acetate=10:1) on silica gel column to give the desired 14-chloro-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoic acid ethyl ester (64.6 mg, 86%) from the desired fraction.
後処理
- customthe organic layer is separated
- washThe organic layer is washed with water
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customThe resulting residue is chromatographed (n-hexane/ethyl acetate=10:1) on silica gel column
出典と根拠
- ORDレコード
- ord-08c8d6224e744d0c8668bf1c9afa5f07
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05292911
関連ノート
読み込み中…