Water → 4,6-Di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran
反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:10][C:11]1[C:12]([C:28]([CH3:31])([CH3:30])[CH3:29])=[CH:13][C:14]2[O:18][C:17]([CH2:21][CH3:22])([CH2:19][CH3:20])[CH2:16][C:15]=2[C:23]=1[C:24]([CH3:27])([CH3:26])[CH3:25])(=O)C.O.[OH-].[Na+]>O1CCCC1>[C:24]([C:23]1[C:15]2[CH2:16][C:17]([CH2:19][CH3:20])([CH2:21][CH3:22])[O:18][C:14]=2[CH:13]=[C:12]([C:28]([CH3:29])([CH3:31])[CH3:30])[C:11]=1[OH:10])([CH3:25])([CH3:27])[CH3:26]参加物
実験手順
Lithium aluminum hydride (76 mg) was suspended in tetrahydrofuran (5 ml) under a nitrogen atmosphere. A solution of 5-acetoxy-4,6-di-tert-butyl-2,2-diethyl-2,3-dihydrobenzofuran (0.17 g, 0.5 mmol) in tetrahydrofuran (5 ml) was added dropwise to the suspension. After heating under reflux for 3 h, the reaction mixture was cooled to room temperature and water was added dropwise. After addition of 1N aqueous sodium hydroxide (5 ml), the mixture was subjected to extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 4,6-di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran [130 mg (yield, 87%)] as a pale yellow oil. Mass 304(M+), 289, 163, 57
後処理
- temperatureAfter heating
- temperatureunder reflux for 3 h
- extractionthe mixture was subjected to extraction with diethyl ether
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- concentrationconcentrated
- customThe concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane)
出典と根拠
- ORDレコード
- ord-4b21c77105324461ab3f27a8b47b9122
- 出典データセット
- uspto-grants-1996_11
- 特許番号
- US05574178
反応ノート
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