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Sulfuric Acid → 2-Fluoro-6-iodobenzaldehyde

HRID 1251150
ノート
印刷プレビュー

反応式

HRID 1251150 の反応式
[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([I:10])[C:3]=1[C:4]#N.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1.S(=O)(=O)(O)[OH:29]>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([I:10])[C:3]=1[CH:4]=[O:29]
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 1118Sulfuric AcidHCID 5227222-Fluoro-6-iodobenzonitrileHCID 86583787Diisobutylaluminumhydride toluene

生成物 1

HCID 110969762-Fluoro-6-iodobenzaldehyde収率 83%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

2-Fluoro-6-iodobenzonitrile (10.274 g) was dissolved in toluene (100 ml), followed by the dropwise addition of 1.5M diisobutylaluminium hydride/toluene solution (31 ml) in nitrogen atmosphere at −70° C., and the mixture was stirred for 25 min. Subsequently, it was stirred at room temperature for further 45 min. To the mixture was added 5% sulfuric acid, and it was stirred for 1 hr. Sequentially, the resulting solution was extracted with ethyl acetate, and the resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a yellow oil (8.683 g, yield; 83%).

後処理

  1. stirringSubsequently, it was stirred at room temperature for further 45 min
  2. stirringwas stirred for 1 hr
  3. extractionSequentially, the resulting solution was extracted with ethyl acetate
  4. washthe resulting organic layer was washed with water
  5. dry with materialdried (over MgSO4)
  6. customevaporated
  7. customThe resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system)

出典と根拠

ORDレコード
ord-01ae5be02623400da963b0d5da28a91a
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06340759B1

反応ノート

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