反応式
[CH2:1]([OH:4])[CH2:2][OH:3].CC(C)=O.[C:9](Cl)(=[O:21])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]>N1C=CC=CC=1>[OH:3][CH2:2][CH2:1][O:4][C:9](=[O:21])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]参加物
5
実験手順
Under cooling with ice, ethylene glycol (434 mg) was dissolved into acetone (20 ml), and pyridine (632 mg) was added thereto and then lauroyl chloride (1532 mg) was added dropwise thereto. The temperature of the solution was warmed to room temperature, and it was stirred for 2 hours. The mixture was evaporated. To the residue was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water (three times), dried over magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1) to give the title compound (1.63 g) having the following physical data.
後処理
- additionwas added
- customThe mixture was evaporated
- additionTo the residue was added water
- extractionthe solution was extracted with ethyl acetate
- washThe organic layer was washed with water (three times)
- dry with materialdried over magnesium sulfate
- customevaporated
- customThe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1)
出典と根拠
- ORDレコード
- ord-7d11efc8ffa84e98977b6dbc75123864
- 出典データセット
- uspto-grants-1997_11
- 特許番号
- US05690957
関連ノート
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