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Hydrochloric Acid → 4-Bromo-6-methoxyquinoline-3-carboxylic acid

HRID 639001
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인쇄 미리보기

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HRID 639001 반응식
C([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[Br:16])=[CH:13][C:12]([O:17][CH3:18])=[CH:11][CH:10]=2)=[O:5])C.[OH-].[Na+].CO.C(Cl)Cl.Cl>C1COCC1>[Br:16][C:15]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([O:17][CH3:18])[CH:13]=2)[N:8]=[CH:7][C:6]=1[C:4]([OH:5])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 21226129Dichloromethane methanolHCID 49758155Ethyl 4-bromo-6-methoxyquinoline-3-carboxylate

생성물 1

HCID 684531854-Bromo-6-methoxyquinoline-3-carboxylic acid수율 91.3%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

4-Bromo-6-methoxy-quinoline-3-carboxylic acid ethyl ester (41 g, 0.132 mole), partially dissolved in THF (600 mL), was treated dropwise with aqueous 2 M sodium hydroxide (198.4 mL, 0.396 mole). After 24 hr, the reaction was complete by TLC (2% MeOH/CH2Cl2). The mixture was neutralized with 5 M HCl then the THF was removed in vacuo. The residue was dissolved in water and acidified with 5 M HCl. The solid product was collected under suction, washed well with water, and dried in vacuo to give the title compound (34 g, 91%) as a white solid: MS (ES) m/e 282/284 (M+H)+.

후처리

  1. customthe THF was removed in vacuo
  2. dissolutionThe residue was dissolved in water
  3. customThe solid product was collected under suction
  4. washwashed well with water
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-81f9e65b74694778aa3dc6b497c25f11
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691850B2

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