反応式
[CH3:1][O:2][CH:3]1[C:8]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH:10]=2)=[CH:7][CH2:6][CH2:5][CH2:4]1>CCOC(C)=O.[Pd]>[CH3:1][O:2][CH:3]1[CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1参加物
4
実験手順
Treat 3-(6-methoxy-cyclohex-1-enyl)-1H-indole (200 mg, 0.879 mmol) with 10% Pd/C (40 mg) in EtOAc under atmospheric hydrogenation conditions for 1.5 hours. Filter resulting solution over Celite to remove catalyst. Concentrate crude on rotovap and purify on silica gel chromatography to give 3-(2-Methoxy-cyclohexyl)-1H-indole (127 mg, 63% yield). Mass Spectrum (m/e): 230.03 (MH+), 228.14 (M−).
後処理
- filtrationFilter
- customresulting solution over Celite
- customto remove catalyst
- concentrationConcentrate crude on rotovap
- custompurify on silica gel chromatography
出典と根拠
- ORDレコード
- ord-683d20d846bf496d957543d5f33f089d
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07595339B2
関連ノート
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