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Water → 5-phenylpyridine-2-carboxylic Acid

HRID 1177971
ノート
印刷プレビュー

反応式

HRID 1177971 の反応式
[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
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 14798Sodium HydroxideHCID 9352765-Phenylpyridine-2-carbonitrile

生成物 1

HCID 27628705-phenylpyridine-2-carboxylic Acid収率 27%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-d91f01daccec44579e53ad05ca7e830d
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07842696B2

反応ノート

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