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Diethyl Ether → 7-Bromo-1-benzofuran

HRID 2266226
ノート
印刷プレビュー

反応式

HRID 2266226 の反応式
C(O[CH:4](OCC)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[Br:13])C.[OH-].[Na+].CCOCC>ClC1C=CC=CC=1>[Br:13][C:8]1[C:7]2[O:6][CH:5]=[CH:4][C:12]=2[CH:11]=[CH:10][CH:9]=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 3

HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 229514321-Bromo-2-(2,2-diethoxyethoxy)benzene

生成物 1

HCID 1136287-Bromo-1-benzofuran収率 38%

試薬・触媒・溶媒 1

HCID 7964Chlorobenzene溶媒2 回

実験手順

A stirred mixture of polyphosphoric acid (˜5 g) and chlorobenzene (8 mL) was heated at reflux and a solution of 1-(2,2-diethoxyethoxy)-2-bromobenzene (2.62 g, 9.0 mmol) in chlorobenzene (3 mL) was added dropwise over 10 min. The mixture was heated at reflux for 1.5 h. The mixture was allowed to cool to rt and 1M aq NaOH (20 mL) was added, followed by ether (175 mL). The mixture was washed with water (2×20 mL) and brine (20 mL), and dried over MgSO4. Evaporation of the solvent left a residue which was purified by a chromatography on a 140-g silica cartridge eluted with hexanes and a 0-10% EtOAc in hexanes gradient. Appropriate fractions were pooled and concentrated to afford 7-bromobenzofuran (0.65 g, 38% from 2-bromophenol) as a clear colorless oil.

後処理

  1. temperaturewas heated
  2. temperatureat reflux
  3. temperatureThe mixture was heated
  4. temperatureat reflux for 1.5 h
  5. washThe mixture was washed with water (2×20 mL) and brine (20 mL)
  6. dry with materialdried over MgSO4
  7. customEvaporation of the solvent
  8. waitleft a residue which
  9. customwas purified by a chromatography on a 140-g silica cartridge
  10. washeluted with hexanes
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-388a6841169e4b118d7ebf45649d8d69
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07858624B2

反応ノート

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