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Hydrogen Bromide → 3-Bromo-5-iodophenol

HRID 1784829
ノート
印刷プレビュー

反応式

HRID 1784829 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([O:8]C)[CH:5]=[C:4]([I:10])[CH:3]=1.Br>C(O)(=O)C.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[Br:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([I:10])[CH:3]=1
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 2

HCID 260Hydrogen BromideHCID 509981531-Bromo-3-iodo-5-methoxybenzene

生成物 1

HCID 226301823-Bromo-5-iodophenol収率 352.9%

試薬・触媒・溶媒 2

HCID 74236Tetrabutylammonium Bromide触媒HCID 176Acetic Acid溶媒

実験手順

1-Bromo-3-iodo-5-methoxy-benzene (6.29 g, 20.1 mmol) was suspended in a solution of hydrogen bromide in acetic acid (33%, 150 mL). Tetrabutylammonium bromide (0.5 g, 1.55 mmol) was added and the mixture was heated to reflux under vigorous stirring for 2 d. After cooling to room temperature the mixture was extracted with methylene chloride (3×100 mL). The combined organic layers were washed with water (50 mL), dried (MgSO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (300 g, AcOEt/heptane 1:9). 3-Bromo-5-iodo-phenol (21.2 g, 96%) was obtained as pale brown solid.

後処理

  1. temperaturethe mixture was heated
  2. temperatureto reflux
  3. extractionwas extracted with methylene chloride (3×100 mL)
  4. washThe combined organic layers were washed with water (50 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customto give the crude product which
  8. customwas purified by flash chromatography on silica gel (300 g, AcOEt/heptane 1:9)

出典と根拠

ORDレコード
ord-c82d30573024422aae1fd2c8d0f47fec
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07504401B2

反応ノート

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