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Water → 5-phenylpyridine-2-carboxylic Acid

HRID 1177971
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HRID 1177971 반응식
[OH2:1].[OH-:2].[Na+].[C:4]1([C:10]2[CH:11]=[CH:12][C:13]([C:16]#N)=[N:14][CH:15]=2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>C(O)C>[C:4]1([C:10]2[CH:11]=[CH:12][C:13]([C:16]([OH:2])=[O:1])=[N:14][CH:15]=2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 9352765-Phenylpyridine-2-carbonitrile

생성물 1

HCID 27628705-phenylpyridine-2-carboxylic Acid수율 27%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Water (1 mL) and NaOH (56 mg, 1.41 mmol) were added to a stirred solution of 5-phenyl-pyridine-2-carbonitrile (112 mg, 0.56 mmol) in ethanol at room temperature. The resulting mixture was heated at reflux temperature for 3 hours. The EtOH was evaporated, and the mixture was diluted with water (2 mL), acidified with citric acid solution and the product was extracted using EtOAc. The organic layer was washed with saturated brine solution, dried over Na2SO4 and concentrated under reduced pressure to afford 30 mg (27% yield) of 5-phenyl-pyridine-2-carboxylic acid.

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후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux temperature for 3 hours
  3. customThe EtOH was evaporated
  4. additionthe mixture was diluted with water (2 mL)
  5. extractionthe product was extracted
  6. washThe organic layer was washed with saturated brine solution
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-d91f01daccec44579e53ad05ca7e830d
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07842696B2

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