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Sodium Hydroxide → 2-(6-Quinolinyloxy)-2-(ethoxy)acetic acid

HRID 1244807
ノート
印刷プレビュー

反応式

HRID 1244807 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([O:11][CH:12]([O:18][CH2:19][CH3:20])[C:13]([O:15]CC)=[O:14])=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>O.CO>[N:1]1[C:10]2[C:5](=[CH:6][C:7]([O:11][CH:12]([O:18][CH2:19][CH3:20])[C:13]([OH:15])=[O:14])=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=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 2

HCID 14798Sodium HydroxideHCID 21923123Ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate

生成物 1

HCID 219231312-(6-Quinolinyloxy)-2-(ethoxy)acetic acid収率 44.5%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

Ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate (3.68 g) was added to a solution of sodium hydroxide (0.589 g) in water (10 ml) and methanol (30 ml) and stirred for 5 minutes. The solution was evaporated under reduced pressure, water added and the aqueous phase was washed with ethyl acetate. The aqueous phase was acidified with hydrochloric acid and extracted with ethyl acetate. The extracts were combined, dried over magnesium sulphate and evaporated under reduced pressure to give 2-(6-quinolinyloxy)-2-(ethoxy)acetic acid (1.47 g) as a cream solid.

後処理

  1. customThe solution was evaporated under reduced pressure, water
  2. additionadded
  3. washthe aqueous phase was washed with ethyl acetate
  4. extractionextracted with ethyl acetate
  5. dry with materialdried over magnesium sulphate
  6. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-d53b720ee3d8486da89b2e13d0a19eb5
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07122672B2

反応ノート

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