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

HRID 2222288
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반응식

HRID 2222288 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

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

생성물 1

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

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-82529aeb338a4274bc76c065460df362
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07371764B2

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