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

HRID 1043414
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HRID 1043414 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-29868b549e6142709f9143c19db7f506
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563505B2

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