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Sulfuric Acid → 2-Bromo-4-iodo-1-methylbenzene

HRID 857375
ノート
印刷プレビュー

反応式

HRID 857375 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])N.S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:19].[K+]>O>[Br:1][C:2]1[CH:3]=[C:4]([I:19])[CH:6]=[CH:7][C:8]=1[CH3:9]
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 4

HCID 1118Sulfuric AcidHCID 4875Potassium IodideHCID 82187Benzenamine, 3-bromo-4-methyl-HCID 23668193Sodium Nitrite

生成物 1

HCID 215600382-Bromo-4-iodo-1-methylbenzene収率 94%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

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
温度
0 °C

実験手順

To a vigorously stirred mixture of 3-bromo-4-methylaniline (40 g, 215 mmol), sulfuric acid (360 mL) and H2O (900 mL) at 0° C. was added dropwise a NaNO2 solution (16.6 g, 240 mmol in 80 mL of H2O). The mixture was stirred at 0° C. for 1 hour and a solution of potassium iodide (64 g, 387 mmol in 160 mL of H2O) was added. The reaction was stirred for 8 hours at r.t. The aqueous layer was extracted with Et2O and the combined organic layers were washed with a 10% aqueous solution of Na2S2O3, dried over Na2SO4 and concentrated. The residue was filtered through a silica gel pad eluted with 10% EtOAc/hexane and concentrated to give 60 g of the title compound as a reddish syrup used as such.

後処理

  1. stirringThe reaction was stirred for 8 hours at r.t
  2. extractionThe aqueous layer was extracted with Et2O
  3. washthe combined organic layers were washed with a 10% aqueous solution of Na2S2O3
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. filtrationThe residue was filtered through a silica gel pad
  7. washeluted with 10% EtOAc/hexane
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-13776f78ed434af0ba6159c5383045ee
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07144913B2

反応ノート

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