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Hydrogen Peroxide → Phenol, 5-bromo-2-fluoro-

HRID 1180264
ノート
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反応式

HRID 1180264 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6](B(O)O)[CH:7]=1.[OH:12]O.[OH-].[Na+]>O1CCCC1.O.[O-2].[O-2].[Mn+4]>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([OH:12])[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

7

反応物 3

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 10856974(5-Bromo-2-fluorophenyl)boronic acid

生成物 1

HCID 183421Phenol, 5-bromo-2-fluoro-収率 90%

試薬・触媒・溶媒 3

HCID 178418406HCID 178418406、化合物触媒HCID 962Water溶媒2 回
HCID 8028
Tetrahydrofuran
溶媒

実験手順

A solution of 5-bromo-2-fluorobenzeneboronic acid (25 g, 114 mmol) in tetrahydrofuran was treated with hydrogen peroxide (7.8 ml of a 35 wt % solution in water) then with sodium hydroxide (1.4 ml of a 4N solution in water). A mild exotherm caused the internal temperature to reach 40° C. This mixture was left to stir at ambient temperature for 14 h then treated with manganese dioxide (200 mg) and stirring was continued for 90 min before filtering the reaction (GF/A filter paper). The filtrate was concentrated on a rotary evaporator and the residue partitioned between ether (400 ml) and water. The organics were washed with more water and brine, and dried over anhydrous magnesium sulphate. Filtration and evaporation to dryness afforded 5-bromo-2-fluorophenol (19.7 g, 90%) as a colourless liquid: δH (400 MHz, d6-DMSO) 6.93-6.97 (1H, m), 7.09-7.14 (2H, m), 10.36 (1H, br).

後処理

  1. customto reach 40° C
  2. waitThis mixture was left
  3. stirringstirring
  4. waitwas continued for 90 min
  5. filtrationbefore filtering
  6. customthe reaction (GF/A filter paper)
  7. concentrationThe filtrate was concentrated on a rotary evaporator
  8. customthe residue partitioned between ether (400 ml) and water
  9. washThe organics were washed with more water and brine
  10. dry with materialdried over anhydrous magnesium sulphate
  11. filtrationFiltration and evaporation to dryness

出典と根拠

ORDレコード
ord-98506153afa7442da2d0fc39837b1b2e
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07279580B2

反応ノート

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