反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]=[O:11].[CH2:12](O)[CH2:13][OH:14].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]1[O:14][CH2:13][CH2:12][O:11]1参加物
5
実験手順
9-Bromononanal (28.0 g, assumed 120 mmol), ethylene glycol (33.6 mL, 600 mmol) and para-toluenesulphonic acid (2.7 g, 13 mmol) in toluene (210 mL) were heated at reflux for 20 hours. The reaction was cooled to RT and quenched with saturated aqueous sodium bicarbonate solution (300 mL). The resulting mixture was extracted with diethyl ether (2×500 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution (300 mL), water (300 mL), brine (100 mL), dried (magnesium sulfate), filtered and evaporated under reduced pressure to afford the title compound (25.2 g, 79%).
後処理
- temperatureat reflux for 20 hours
- customquenched with saturated aqueous sodium bicarbonate solution (300 mL)
- extractionThe resulting mixture was extracted with diethyl ether (2×500 mL)
- washThe combined organic extracts were washed with saturated aqueous sodium bicarbonate solution (300 mL), water (300 mL), brine (100 mL)
- dry with materialdried (magnesium sulfate)
- filtrationfiltered
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-a4c714a186604d398b6b4ba90372980c
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877774B2
関連ノート
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