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Hydrochloric Acid → 3-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

HRID 2232647
ノート
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反応式

HRID 2232647 の反応式
[Br:1][C:2]1[C:8]([F:9])=[C:7]([F:10])[CH:6]=[C:5]([N+:11]([O-:13])=[O:12])[C:3]=1N.C(ON=O)(C)(C)C.[ClH:21]>C(#N)C>[Br:1][C:2]1[C:3]([Cl:21])=[C:5]([N+:11]([O-:13])=[O:12])[CH:6]=[C:7]([F:10])[C:8]=1[F:9]
参加物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 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 140717912-Bromo-3,4-difluoro-6-nitroaniline

生成物 1

HCID 140717923-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a mixture of anhydrous cupric chloride (3.1 g) and 2-bromo-3,4-difluoro-6-nitroaniline (4.6 g) in anhydrous acetonitrile (30 ml) was added t-butylnitrite (2.8 g) dropwise at 51° to 56° C. during 5 minutes. After stirring for 8 minutes at the same temperature, the reaction mixture was poured into chilled 10% diluted hydrochloric acid (30 ml) and extracted with benzene. The organic layer was washed with diluted hydrochloric acid and with water successively, dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified by silica gel chromatography eluting with dichloromethane-n-hexane (1:5) to give the title compound (4.0 g).

後処理

  1. additionthe reaction mixture was poured
  2. extractionextracted with benzene
  3. washThe organic layer was washed with diluted hydrochloric acid and with water successively
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe resulting residue was purified by silica gel chromatography
  7. washeluting with dichloromethane-n-hexane (1:5)

出典と根拠

ORDレコード
ord-503409b5706a49a087dc5e93e6199ad0
出典データセット
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04788320

反応ノート

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