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Water → 4-Bromo-[1,1'-biphenyl]-2-carboxylic acid

HRID 1043414
ノート
印刷プレビュー

反応式

HRID 1043414 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:4]([CH3:14])[CH:3]=1.[Mn]([O-])(=O)(=O)=[O:16].[K+].[OH2:21]>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([C:14]([OH:16])=[O:21])[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][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

5

反応物 3

HCID 962WaterHCID 516875Potassium PermanganateHCID 99648454-Bromo-2-methylbiphenyl

生成物 1

HCID 199224694-Bromo-[1,1'-biphenyl]-2-carboxylic acid収率 89%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

4-bromo-2-methylbiphenyl (5 g, 20.23 mmol) was suspended in pyridine (23 mL) and water (35 mL). Potassium permanganate (16 g, 101 mmol) was added portion wise over a period of 20 min. The mixture was refluxed overnight. The reaction mixture was cooled and MnO2 was filtered off. Conc. HCl was added to the filtrate until the product precipitated. The product was extracted with DCM, washed with water and brine, collected, dried (MgSO4), filtered and evaporated to give 4-bromobiphenyl-2-carboxylic acid (5 g, 18.04 mmol, 89% yield) as a white solid. LCMS: rt=1.39 min.; Phenomenex-Luna C-18 (5μ) (3.0×50 mm); Solvent A=10% acetonitrile—90% water—0.1% TFA, Solvent B=90% acetonitrile—10% water—0.1% TFA; gradient 0% to 100% solvent B over 2 min. and then hold for 1 min.; 4 mL/min; inj. vol.=5 uL; wavelength=220.

後処理

  1. temperatureThe mixture was refluxed overnight
  2. temperatureThe reaction mixture was cooled
  3. filtrationMnO2 was filtered off
  4. additionConc. HCl was added to the filtrate until the product
  5. customprecipitated
  6. extractionThe product was extracted with DCM
  7. washwashed with water and brine
  8. customcollected
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. customevaporated

出典と根拠

ORDレコード
ord-29868b549e6142709f9143c19db7f506
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08563505B2

反応ノート

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