反応式
Cl[C:2](Cl)(Cl)[CH:3]([OH:5])O.S([O-])([O-])(=O)=O.[Na+].[Na+].Cl.[NH2:16][OH:17].Cl.[NH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>O>[N:16](=[CH:2][C:3]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:5])[OH:17]参加物
7
実験手順
25 mL H2O was added to chloral hydrate (1.49 g, 9 mmol) and anhydrous sodium sulfate (7.62 g, 54 mmol), and the mixture was rapidly stirred until clear. Hydroxylamine hydrochloride (6.84 g, 42 mmol) was added into dilute hydrochloric acid (9 mL H2O: 1 mL concentrated HCl), and then, aniline (1.23 g, 8 mmol) was added. The mixture was stirred to form a suspension. The suspension was added into an aqueous solution of chloral hydrate. After stirring for 5 min, the mixture was transferred to an oil bath at 45° C. and heated for 2 h. The reaction was finished by TLC detection, and the reaction system was stirred and cooled in an ice bath, filtered and dried, to obtain a solid oximino acetanilide.
後処理
- stirringThe mixture was stirred
- customto form a suspension
- stirringAfter stirring for 5 min
- customthe mixture was transferred to an oil bath at 45° C.
- temperatureheated for 2 h
- stirringthe reaction system was stirred
- temperaturecooled in an ice bath
- filtrationfiltered
- customdried
出典と根拠
- ORDレコード
- ord-2668a1dd7ba04ab49a00afdb15bdafc1
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181193B2
関連ノート
読み込み中…