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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428537생성일: 2026년 10월 23일

6-Methoxyquinoline → 5-Bromo-6-methoxyquinoline

https://huagongshe.com/ko/reaction/428537

반응식

참여 물질

역할이름HCID투입량
반응물6-MethoxyquinolineHCID 14860—
반응물BromineHCID 24408—
반응물Sodium BisulfiteHCID 23665763—
용매Acetic AcidHCID 176—
생성물5-Bromo-6-methoxyquinolineHCID 1841412858.7%

반응 단계

To a solution of 6-methoxyquinoline (5 g, 31.4 mmol) in acetic acid (50 mL) was slowly added Br2 neat (1.62 mL, 31.4 mmol). The reaction mixture was stirred at ambient temperature for 1 hour and then poured onto ice. Saturated aqueous sodium bisulfite was added, and the resulting slurry was extracted into EtOAc (2×200 mL). The organic fractions were combined, dried over Na2SO4, concentrated, and purified by column chromatography (5% MeOH/CH2Cl2) affording 4.39 g of the title compound as the acetate salt. The free base was prepared by washing the salt with 1 N NaOH (50 mL) and H2O (100 mL) and extracting into CH2Cl2 (200 mL). The organic fractions were concentrated affording 3.89 g (52%) of the title compound as a pink solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313126B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-04db3afc05d0439e8c9082b013422ddd
출처 메모uspto-grants-2001_11