反応式
Cl.[N+:2]([C:5]1[CH:15]=[CH:14][C:8]([O:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:7][CH:6]=1)([O-:4])=[O:3].[CH2:16](O)[CH2:17][OH:18]>>[OH:18][CH2:17][CH2:16][O:12][C:11](=[O:13])[CH2:10][O:9][C:8]1[CH:7]=[CH:6][C:5]([N+:2]([O-:4])=[O:3])=[CH:15][CH:14]=1参加物
4
実験手順
Dry HCl gas was passed through a mixture of (4-nitrophenoxy)acetic acid 22 (100 g, 507 mmol) and ethylene glycol (300 ml) for 1 hour. During HCl gas bubbling the temperature rose to 60° C. The crude reaction mass was poured onto ice (2 kg). Crude 23 was filtered, dried and purified by column chromatography on silica gel using hexane:ethyl acetate (95:5) to give pure 23 (70 g, 57.4%) as a white powder with an m.p. between 73.5-75.5° C.
後処理
- customDuring HCl gas bubbling the temperature
- customrose to 60° C
- customThe crude reaction mass
- additionwas poured onto ice (2 kg)
- filtrationCrude 23 was filtered
- customdried
- custompurified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-1c5655145141470a8899330a915486d4
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846845B2
関連ノート
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