反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].S(=O)(=O)(O)O.[H-].[Al+3].[H-].[H-].[Br:16][C:17]1[CH:22]=[CH:21][C:20]([CH:23]([C:31]([N:33]([CH3:35])[CH3:34])=O)[C:24]2([OH:30])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]2)=[CH:19][CH:18]=1.[OH-].[Na+]>C1COCC1.C1COCC1.O>[Br:16][C:17]1[CH:18]=[CH:19][C:20]([CH:23]([C:24]2([OH:30])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]2)[CH2:31][N:33]([CH3:35])[CH3:34])=[CH:21][CH:22]=1参加物
反応条件
- 温度
- 0 °C
実験手順
Lithium aluminum hydride (0.7 g) was suspended in dry THF (25 ml) cooled to 0° C. and concentrated sulfuric acid (0.5 ml) cautiously added in an in situ preparation of aluminum hydride. The mixture was stirred for one hour at 0° C. and the amide, 1-[(4-bromophenyl)[dimethylaminocarbonyl]methyl]cyclohexanol (4 g, 0.012 mole) was dissolved in THF (35 ml) and added rapidly dropwise. The reaction mixture was stirred at 0° C. for one hour. A THF-water mixture (1:1 v/v 6 ml) was added slowly followed by 10% sodium hydroxide (10 ml). The mixture was filtered and the residue washed well with ethyl acetate. The combined filtrate was dried over anhydrous potassium carbonate and evaporated to an oil (3.5 g) which was converted to the hydrochloride salt using 4 N isopropanolic HCl.
後処理
- additionadded rapidly dropwise
- stirringThe reaction mixture was stirred at 0° C. for one hour
- filtrationThe mixture was filtered
- washthe residue washed well with ethyl acetate
- dry with materialThe combined filtrate was dried over anhydrous potassium carbonate
- customevaporated to an oil (3.5 g) which
出典と根拠
- ORDレコード
- ord-6caa22fbf96d454c889b849950738325
- 出典データセット
- uspto-grants-1988_08
- 特許番号
- US04761501
関連ノート
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