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Ethyl Acetate → 2,5-Dibromo-3,6-difluoroaniline

HRID 1270740
ノート
印刷プレビュー

反応式

HRID 1270740 の反応式
[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([Br:9])=[C:4]([F:10])[C:3]=1[N+:11]([O-])=O.CCOC(C)=O>C(O)C.Cl.[Fe]>[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([Br:9])=[C:4]([F:10])[C:3]=1[NH2:11]
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

6

反応物 2

HCID 8857Ethyl AcetateHCID 184514931,4-Dibromo-2,5-difluoro-3-nitrobenzene

生成物 1

HCID 184514922,5-Dibromo-3,6-difluoroaniline

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 313Hydrochloric Acid溶媒HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

2,5-Dibromo-3,6-difluoronitrobenzene (120 g, 0.37 mol) is dissolved in a mixture of ethanol (300 mL) and concentrated HCl (500 mL). The mixture is heated to 80° C. and treated with iron powder (100 g, 1.78 mol) by portion-wise addition over 2 hours. After stirring for an additional hour, the mixture is cooled to room temperature and EtOAc (800 mL) is added. The solids are removed by filtration and then the solution concentrated by rotary evaporator to remove most of the solvent. The residue is partitioned between EtOAc (1000 mL) and water (500 mL). The organic layer is washed with brine (2×250 mL), dried (MgSO4) and concentrated by rotary evaporator to give a brown oil. The crude product is then purified using flash chromatography (9:1 hexanes/EtOAc) to give 2,5-dibromo-3,6-difluoroaniline.

後処理

  1. temperaturethe mixture is cooled to room temperature
  2. customThe solids are removed by filtration
  3. concentrationthe solution concentrated by rotary evaporator
  4. customto remove most of the solvent
  5. customThe residue is partitioned between EtOAc (1000 mL) and water (500 mL)
  6. washThe organic layer is washed with brine (2×250 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated by rotary evaporator
  9. customto give a brown oil
  10. customThe crude product is then purified

出典と根拠

ORDレコード
ord-7cf0a0c661de42a19af0ec90263fae5f
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07202364B2

反応ノート

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