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Sodium Hydroxide → 7-Methoxyquinoline-3-carboxylic acid

HRID 495478
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HRID 495478 반응식
Cl.[CH3:2][O:3][C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[C:9]([C:14]([O:16]CC)=[O:15])[CH:10]=[N:11]2)=[CH:6][CH:5]=1.[OH-].[Na+]>CCO>[CH3:2][O:3][C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[C:9]([C:14]([OH:16])=[O:15])[CH:10]=[N:11]2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 223268747-Methoxy-3-ethoxycarbonylquinoline hydrochloride

생성물 1

HCID 146728247-Methoxyquinoline-3-carboxylic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a stirred solution of 7-methoxy-3-ethoxycarbonylquinoline hydrochloride (Step C, 1.45 g, 5.4 mmol) in EtOH (24 mL) was added at RT 2N NaOH (8 mL, 16 mmol). The reaction was stirred at RT overnight. After concentration under vacuum, the mixture was acidified with 1N HCl. The resulting solid was filtered off, washed with water and dried over P2O5 to give 7-methoxy-3-carboxyquinoline.

후처리

  1. concentrationAfter concentration under vacuum
  2. filtrationThe resulting solid was filtered off
  3. washwashed with water
  4. dry with materialdried over P2O5

출처 및 근거

ORD 기록
ord-c39495bfa0a2429992f8d4b3cad26284
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06939874B2

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