反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:7]([CH2:14][CH2:15][C:16](O)=[O:17])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O.[OH-].[Na+]>C(OCC)C>[O:7]([CH2:14][CH2:15][CH2:16][OH:17])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
実験手順
To a stirred suspension of 5.7 g (0.15 mole) of lithium aluminum hydride in 350 ml of dry ethyl was added dropwise (30 min) a solution of 25.0 g (0.149 mole) of 3-phenoxypropionic acid (99%, Aldrich Chem. Co.) in 250 ml of dry ethyl ether. The reaction mixture was stirred at ambient temperature for 2 hr and treated successively with 6 ml of water, 18 ml of a 15% sodium hydroxide solution, and 10 ml of water. The reaction mixture was filtered through Celite® and the filtrate was concentrated to a viscous residue. The residue was partitioned between water and ethyl ether (300 ml each). The ethereal layer was washed with two 300 ml portions of water, dried over magnesium sulfate and the solvent was evaporated under reduced pressure to give 16.6 g (73%) of colorless oil.
後処理
- filtrationThe reaction mixture was filtered through Celite®
- concentrationthe filtrate was concentrated to a viscous residue
- customThe residue was partitioned between water and ethyl ether (300 ml each)
- washThe ethereal layer was washed with two 300 ml portions of water
- dry with materialdried over magnesium sulfate
- customthe solvent was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-132d40c9e4494fde875d81e7446d7560
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05273993
関連ノート
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