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Water → 4-Bromo-2,3-difluoro-6-nitroaniline

HRID 1245438
ノート
印刷プレビュー

反応式

HRID 1245438 の反応式
[F:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[C:3]=1[NH2:4].[Br:13]N1C(=O)CCC1=O.O>CN(C)C=O>[Br:13][C:7]1[CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[C:3]([NH2:4])=[C:2]([F:1])[C:8]=1[F:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 27370282,3-Difluoro-6-nitroaniline

生成物 1

HCID 219119704-Bromo-2,3-difluoro-6-nitroaniline収率 73.6%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

To a solution of 3.00 g of 2,3-difluoro-6-nitroaniline in 30 ml of dimethylformamide, 6.14 g of N-bromosuccinimide was added, followed by an hour's stirring at 90° C. Water was added to the reaction liquid which then was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried on anhydrous magnesium sulfate and the solvent was distilled off. The residue was separated and purified on silica gel column chromatography (ethyl acetate/hexane=1/6) to provide 3.21 g of the title compound.

後処理

  1. waitfollowed by an hour
  2. extractionthen was extracted with ethyl acetate
  3. washThe ethyl acetate layer was washed with saturated brine
  4. dry with materialdried on anhydrous magnesium sulfate
  5. distillationthe solvent was distilled off
  6. customThe residue was separated
  7. custompurified on silica gel column chromatography (ethyl acetate/hexane=1/6)

出典と根拠

ORDレコード
ord-d29a8d73498f49718b3ea887a037f176
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07125877B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート