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Sodium Hydroxide → 4-Trifluoroacetylaniline

HRID 28628
ノート
印刷プレビュー

反応式

HRID 28628 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-])=O)=[CH:7][CH:6]=1)=[O:4].[Sn](Cl)Cl.[OH-].[Na+]>Cl.O>[NH2:11][C:8]1[CH:9]=[CH:10][C:5]([C:3](=[O:4])[C:2]([F:1])([F:14])[F:15])=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14798Sodium HydroxideHCID 24479Stannous ChlorideHCID 110639262,2,2-Trifluoro-1-(4-nitrophenyl)ethanone

生成物 1

HCID 901384-Trifluoroacetylaniline収率 19.3%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 962Water溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

To a suspension of 2,2,2-trifluoro-1-(4-nitro-phenyl)-ethanone (4.5 g, 20.5 mmol) in concentrated hydrochloric acid (15 ml) and water (15 ml) was added tin (II) chloride (14 g, 74 mmol). After stirring for 24 hours, the mixture was adjusted to pH 10 by addition of aqueous sodium hydroxide solution (50%) and extracted with ethyl acetate. The organic extract was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:5) followed by recrystallization (ethyl acetate-hexane) to afford 1-(4-amino-phenyl)-2,2,2-trifluoro-ethanone (750 mg, 19% yield).

後処理

  1. extractionextracted with ethyl acetate
  2. extractionThe organic extract
  3. concentrationwas concentrated under reduced pressure
  4. customThe residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:5)
  5. customfollowed by recrystallization (ethyl acetate-hexane)

出典と根拠

ORDレコード
ord-4c0bbe7599784a49a6c3c401377c1fa1
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07419984B2

反応ノート

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