Cyclohexene → 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxyindole
反応式
[CH2:1]([C:4]1[C:5]([O:19][CH3:20])=[C:6]([CH:11]=[C:12]([Cl:18])[C:13]=1[NH:14][C:15](=[O:17])[CH3:16])[C:7]([O:9][CH3:10])=[O:8])[CH:2]=C.I([O-])(=O)(=O)=O.[Na+].C1CCCCC=1>C(O)CCC.O.O1CCOCC1.O.C(O)(C(F)(F)F)=O.C(Cl)Cl.[Os](=O)(=O)(=O)=O>[C:15]([N:14]1[C:13]2[C:4](=[C:5]([O:19][CH3:20])[C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:11][C:12]=2[Cl:18])[CH:1]=[CH:2]1)(=[O:17])[CH3:16]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 6
実験手順
A 2.5% solution of osmium tetroxide in butanol (0.25 ml) is added to a stirred solution of the methoxy compound from step 7 above (1.5 g) in H2O-dioxane (15 ml/45 ml) and stirred for 30 minutes. Sodium periodate (2.25 g) is added portionwise over one hour and the reaction mixture stirred for 31/2 hours. Cyclohexene (1 ml) is added, the mixture stirred for one hour, diluted with H2O and extracted with CHCl3. The organic layer is separated, dried (MgSO4) and evaporated affording a gum which is dissolved in TFA and allowed to stand for 15 minutes. The acid solution is diluted to 100 mls with CH2Cl2 and washed with H2O, saturated NaHCO3, dried (MgSO4) and evaporated affording a solid which is chromatographed on silica gel affording a colorless solid which is the indole as confirmed by NMR (270 MHz, CDCl2).
後処理
- stirringthe reaction mixture stirred for 31/2 hours
- stirringthe mixture stirred for one hour
- extractionextracted with CHCl3
- customThe organic layer is separated
- dry with materialdried (MgSO4)
- customevaporated
- customaffording a gum which
- waitto stand for 15 minutes
- washwashed with H2O, saturated NaHCO3
- dry with materialdried (MgSO4)
- customevaporated
- customaffording a solid which
- customis chromatographed on silica gel affording a colorless solid which
出典と根拠
- ORDレコード
- ord-f06df5c50ee24a2c8fa824502159fc97
- 出典データセット
- uspto-grants-1990_04
- 特許番号
- US04920219
反応ノート
読み込み中…