Hydrochloric Acid → 2-hydroxyimino-N-phenylacetamide

HRID 709385

反応式

HRID 709385 の反応式
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

  1. stirringThe mixture was stirred
  2. customto form a suspension
  3. stirringAfter stirring for 5 min
  4. customthe mixture was transferred to an oil bath at 45° C.
  5. temperatureheated for 2 h
  6. stirringthe reaction system was stirred
  7. temperaturecooled in an ice bath
  8. filtrationfiltered
  9. 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

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