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Sodium Hydroxide → 2-(quinolin-8-yloxy)propanoic acid

HRID 1429466
ノート
印刷プレビュー

反応式

HRID 1429466 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[O:11][CH:12]([CH3:18])[C:13]([O:15]CC)=[O:14])[CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>CCO.O>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[O:11][CH:12]([CH3:18])[C:13]([OH:15])=[O:14])[CH:4]=[CH:3][CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 61723548HCID 61723548、化合物

生成物 1

HCID 28935152-(quinolin-8-yloxy)propanoic acid収率 80.6%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

反応条件

温度
27 °C

実験手順

To a solution of ethyl 2-(quinolin-8-yloxy)propanoate (100 mg, 0.4 mmol) in EtOH (1 ml) was added a solution of NaOH (24 mg, 0.6 mmol) in H2O (0.5 ml) at 27° C. The mixture was stirred for 30 min at 27° C. The mixture was then concentrated and the residue treated with water (5 mL) and extracted with ethyl acetate (2×5 mL). The water layer was then treated with 2N HCl until pH 3 before being extracted with ethyl acetate (2×5 ml). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated to give the title product (70 mg, 80.5%) as a white solid which was used in next step without further purification.

後処理

  1. concentrationThe mixture was then concentrated
  2. additionthe residue treated with water (5 mL)
  3. extractionextracted with ethyl acetate (2×5 mL)
  4. additionThe water layer was then treated with 2N HCl until pH 3
  5. extractionbefore being extracted with ethyl acetate (2×5 ml)
  6. washThe organic layer was washed with brine (30 mL)
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-670d4439d5a74691a02c5c7a9c446081
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08940726B2

反応ノート

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