Hydrochloric Acid → 4-Bromo-1-chloro-2-iodobenzene

HRID 28660

反応式

HRID 28660 の反応式
N(OC(C)(C)C)=O.[Br:8][C:9]1[CH:14]=[CH:13][C:12](N)=[C:11]([I:16])[CH:10]=1.[ClH:17]>C(#N)C.[Cu](Cl)Cl>[Br:8][C:9]1[CH:14]=[CH:13][C:12]([Cl:17])=[C:11]([I:16])[CH:10]=1

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 8239344-Bromo-2-iodoaniline

生成物 1

HCID 510000714-Bromo-1-chloro-2-iodobenzene収率 76%

試薬・触媒・溶媒 2

HCID 24014Cupric Chloride触媒HCID 6342Acetonitrile溶媒2 回

反応条件

温度
60 °C

実験手順

To a stirred suspension of copper (II) chloride (1.62 g, 12.0 mmol) and tert-butyl nitrite (15.0 mmol) in acetonitrile (40 ml), heated at 60° C., was added a solution of 4-bromo-2-iodo-phenylamine (2.98 g, 10.0 mmol) in acetonitrile (10 ml) dropwise over 50 minutes. After stirring at 60° C. for 1 hour, the mixture was poured into 20% hydrochloric acid (200 ml) and extracted with ether (2×30 ml). The crude product was purified by flash chromatography on silica gel eluting with hexane to provide 4-bromo-1-chloro-2-iodo-benzene (2.4 g, 76% yield).

後処理

  1. extractionextracted with ether (2×30 ml)
  2. customThe crude product was purified by flash chromatography on silica gel eluting with hexane

出典と根拠

ORDレコード
ord-56d0793c4c3147fab76e56c4397753b3
出典データセット
uspto-grants-2008_09
特許番号
US07419984B2

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