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Ethanol → 4-Bromo-3-fluorobenzene-1,2-diamine

HRID 1411394
ノート
印刷プレビュー

反応式

HRID 1411394 の反応式
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([N+:9]([O-])=O)[C:3]=1[F:12].CCO.O.[Cl-].[NH4+]>C1COCC1.[Fe]>[Br:1][C:2]1[C:3]([F:12])=[C:4]([NH2:9])[C:5]([NH2:6])=[CH:7][CH:8]=1
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

7

反応物 4

HCID 702EthanolHCID 962WaterHCID 25517Ammonium ChlorideHCID 27831584-bromo-3-fluoro-2-nitroaniline

生成物 1

HCID 27832034-Bromo-3-fluorobenzene-1,2-diamine収率 84%

試薬・触媒・溶媒 2

HCID 23925Iron触媒
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
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
80 °C

実験手順

To a solution of 4-bromo-3-fluoro-2-nitroaniline (3.0 g, 12.8 mmol) in THF (30 mL) was added EtOH (30 mL) and H2O (10 mL) followed by iron powder (3.6 g, 63.8 mmol) and ammonium chloride (1.0 g, 19.2 mmol). The resulting mixture was stirred at 80° C. for 16 hours. The mixture was cooled to room temperature and filtered through diatomaceous earth. The solid was washed with EtOH until no further color came through the filter. The filtrate was concentrated in vacuo and the crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane to give the title compound (2.2 g, 84%).

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through diatomaceous earth
  3. washThe solid was washed with EtOH until no further color
  4. concentrationThe filtrate was concentrated in vacuo
  5. customthe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane

出典と根拠

ORDレコード
ord-ef777020a9f746c69451d7b6adb84f9f
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08921514B2

反応ノート

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