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Water → 6-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

HRID 2095856
ノート
印刷プレビュー

反応式

HRID 2095856 の反応式
[CH2:1]([C:3]1[N:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[C:7](=[O:16])[C:6]([C:17]#N)=[CH:5][CH:4]=1)[CH3:2].[OH2:19].[OH-:20].[Na+]>S(=O)(=O)(O)O>[CH2:1]([C:3]1[N:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[C:7](=[O:16])[C:6]([C:17]([OH:20])=[O:19])=[CH:5][CH:4]=1)[CH3:2]
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 669688016-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

生成物 1

HCID 581586366-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid収率 78%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

A solution of 6-ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile (410 mg, 1.69 mmol) in conc. sulfuric acid (2 mL)/water (2 mL) was stirred at 120° C. for 17 hr. The reaction solution was allowed to cool to room temperature, 6N aqueous sodium hydroxide solution was added, and the aqueous layer was washed with ethyl acetate. 1N Hydrochloric acid was added to the aqueous layer, and the precipitate was collected by filtration and washed with water to give the title compound (345 mg, 78%) as a white solid.

後処理

  1. washthe aqueous layer was washed with ethyl acetate
  2. addition1N Hydrochloric acid was added to the aqueous layer
  3. filtrationthe precipitate was collected by filtration
  4. washwashed with water

出典と根拠

ORDレコード
ord-9c27cc78d92b49f5b8c9fa6e908c254b
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08445509B2

反応ノート

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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