反応式
[CH2:1]([OH:3])[CH3:2].C(OO[C:10](CC)([NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)C)(=O)C=C.[S:21]([C:25]1[CH:30]=[CH:29][C:28]([NH:31][NH2:32])=[CH:27][CH:26]=1)([OH:24])(=[O:23])=[O:22].C(N(CC)CC)C>C(O)(=O)C>[NH:12]([C:10]1[NH:32][N:31]([C:28]2[CH:29]=[CH:30][C:25]([S:21]([OH:24])(=[O:22])=[O:23])=[CH:26][CH:27]=2)[C:1](=[O:3])[CH:2]=1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1参加物
6
実験手順
Into 1.5 l of ethanol were dispersed 118 g of ethylβ-anilino-β-ethoxy acrylate and 94 g of p-sulfophenylhydrazine, and 150 g of triethylamine and glacial acetic acid were successively dropped thereinto while heating (95°-100° C.) and stirring. After heating (95°-100° C.) and stirring for 5 hours, the reaction solution was concentrated under reduced pressure. To the residue so concentrated were added 50 ml of water and 120 ml of ethanol containing 35% by wt. hydrogen chloride to provide a uniform solution. This uniform solution was allowed to stand in a refrigerator for one day and one night. The crystals of the objective compound which precipitated had a melting point of 290° to 291° C. and weighed 145 g.
後処理
- additionwere successively dropped
- temperaturewhile heating (95°-100° C.)
- temperatureAfter heating (95°-100° C.)
- stirringstirring for 5 hours
- concentrationthe reaction solution was concentrated under reduced pressure
- concentrationTo the residue so concentrated
- additionwere added 50 ml of water and 120 ml of ethanol containing 35% by wt. hydrogen chloride
- customto provide a uniform solution
- customThe crystals of the objective compound which precipitated
出典と根拠
- ORDレコード
- ord-8f94abe7944a45dd8559084c155330ef
- 出典データセット
- uspto-grants-1980_02
- 特許番号
- US04188489
関連ノート
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