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Water → 3-(2-Quinolinyl)-2-propenoic acid

HRID 655877
ノート
印刷プレビュー

反応式

HRID 655877 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1/[CH:11]=[CH:12]/[C:13]([O:15]C)=[O:14].O.[OH-].[Na+]>CO>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1/[CH:11]=[CH:12]/[C:13]([OH:15])=[O:14]
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 962Water2 回HCID 14798Sodium HydroxideHCID 6479253Methyl (E)-3-(2-quinolinyl)-2-propenoate

生成物 1

HCID 7129193-(2-Quinolinyl)-2-propenoic acid収率 49%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of methyl (E)-3-(2-quinolinyl)-2-propenoate (2) (1.07 g, 5.02 mmol) in methanol (24 ml), a water solution of 1N NaOH (16 ml, 16.0 mmol) was added and the reaction mixture was stirred at room temperature for 3.5 hours. The mixture was supplemented with water (40 ml) and washed with ethyl acetate (40 ml). The aqueous layer was separated and the pH of the medium was brought to 5. The mixture was extracted with ethyl acetate (3×40 ml) and the combined extracts were dried (Na2SO4). The solvent was evaporated and the residue was dried in vacuum to give the title compound (0.49 g, 49%) as viscous oil. 1H NMR (DMSO-d6, HMDSO), δ: 7.02 (1H, d, J=15.7 Hz); 7.52-8.15 (5H, m); 7.75 (1H, d, J=15.7 Hz); 8.42 (1H, d, J=9.0 Hz); 12.69 (1H, br s).

後処理

  1. washwashed with ethyl acetate (40 ml)
  2. customThe aqueous layer was separated
  3. extractionThe mixture was extracted with ethyl acetate (3×40 ml)
  4. dry with materialthe combined extracts were dried (Na2SO4)
  5. customThe solvent was evaporated
  6. customthe residue was dried in vacuum

出典と根拠

ORDレコード
ord-17449bb7288f48d39ec6a1992001dc46
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071620B2

反応ノート

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