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1-(5-Bromo-2-fluorophenyl)ethanol → 1-(5-Bromo-2-fluorophenyl)ethanone

HRID 490088
ノート
印刷プレビュー

反応式

HRID 490088 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([CH:8]([OH:10])[CH3:9])[CH:7]=1>O1CCOCC1.[O-2].[O-2].[Mn+4]>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 441820551-(5-Bromo-2-fluorophenyl)ethanol

生成物 1

HCID 226074761-(5-Bromo-2-fluorophenyl)ethanone収率 92.1%

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒HCID 312751,4-Dioxane溶媒

実験手順

To a solution of 1-(5-bromo-2-fluoro-phenyl)-ethanol 102 (105 g, 0.479 mol.) in dioxane (2 L) was added manganese dioxide (203 g, 2.35 mol.). The reaction mixture was heated under reflux for 5 hours. The reaction mixture was allowed to cool to room temperature. The reaction mixture was filtered through Celite (i.e., diatomaceous earth) and the solid was washed with ether (1 L). The combined filtrate was evaporated under reduced pressure to afford the 1-(5-bromo-2-fluoro-phenyl)-ethanone 103 (95.7 g, 0.441 mol.) which was used in the next step without further purification.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for 5 hours
  3. filtrationThe reaction mixture was filtered through Celite (i.e., diatomaceous earth)
  4. washthe solid was washed with ether (1 L)
  5. customThe combined filtrate was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-bdd85ab70f194254afbddf83ff28da8c
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07528132B2

反応ノート

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