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Hydrochloric Acid → N-(2-chloro-3-methoxyphenyl)-2-hydroxyimino-acetamide

HRID 420070
ノート
印刷プレビュー

反応式

HRID 420070 の反応式
S([O-])([O-])(=O)=O.[Na+].[Na+].Cl[C:9](Cl)(Cl)[CH:10]([OH:12])O.Cl.[Cl:16][C:17]1[C:23]([O:24][CH3:25])=[CH:22][CH:21]=[CH:20][C:18]=1[NH2:19].Cl.[NH2:27][OH:28]>O>[Cl:16][C:17]1[C:23]([O:24][CH3:25])=[CH:22][CH:21]=[CH:20][C:18]=1[NH:19][C:10](=[O:12])[CH:9]=[N:27][OH:28]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 787HydroxylamineHCID 2707Chloral HydrateHCID 24436Sodium SulfateHCID 248201302-Chloro-3-methoxyaniline hydrochloride

生成物 1

HCID 86633207N-(2-chloro-3-methoxyphenyl)-2-hydroxyimino-acetamide

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
2 回

実験手順

To a stirred solution of sodium sulfate (58.5 g, 412 mmol) in water (100 mL) was added a solution of chloralhydrate (9.36 g, 56.6 mmol) in water (120 mL). Chloroanisidine 39d (10 g, 51.5 mmol) was added followed by 37% HCl (20 mL). A solution of hydroxylamine (50% in water, 4.7 mL, 154.5 mmol) in 50 mL was then added and the reaction mixture was refluxed for 90 min. The suspended solid was filtered off, and washed with water and ether. Organics were dried over Na2SO4, filtered, and concentrated under reduced pressure to yield compound 102d as a brown solid.

後処理

  1. temperaturethe reaction mixture was refluxed for 90 min
  2. filtrationThe suspended solid was filtered off
  3. washwashed with water and ether
  4. dry with materialOrganics were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-e09f404761c948b18d6283553df63389
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093379B2

反応ノート

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