Tetrahydrofuran → Methoxyindoline
反応式
C([N:4]1[C:12]2[C:7](=[C:8](C)[C:9](OC)=[C:10](C)[CH:11]=2)[CH:6](C)[CH2:5]1)(=O)C.C([BH-](CC)CC)C.[Li+].[O:26]1CCC[CH2:27]1>>[CH3:27][O:26][N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][CH2:5]1参加物
実験手順
To an ice-cold solution of indoline 9 (377 mg, 1.6 mmol) dissolved in tetrahydrofuran (5 mL) and kept under an argon atmosphere was added lithium triethylborohydride (3.2 mL, 3.2 mmol), and the mixture was stirred over the range of 0° C. to room temperature for 20 h. The reaction mixture was quenched with 3N hydrochloric acid, and volatiles were removed under vacuum. The resulting solution was acidified to pH 2 with additional 3N hydrochloric acid and washed with methylene chloride. The aqueous solution was basified with saturated aq. sodium bicarbonate and extracted with methylene chloride. The organic extracts were washed with brine and dried (MgSO4). Removal of solvents gave crude methoxyindoline (200 mg, 65% yield) as a brownish yellow oil, which was used without further purification.
後処理
- customThe reaction mixture was quenched with 3N hydrochloric acid, and volatiles
- customwere removed under vacuum
- washwashed with methylene chloride
- extractionextracted with methylene chloride
- washThe organic extracts were washed with brine
- dry with materialdried (MgSO4)
- customRemoval of solvents
出典と根拠
- ORDレコード
- ord-c308900fe55340dd8bb9eec128e4c616
- 出典データセット
- uspto-grants-1997_10
- 特許番号
- US05674876
反応ノート
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