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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519839생성일: 2026년 10월 26일

Ethyl bromoacetate → ethyl 2-(6-bromo-2-oxoquinolin-1(2H)-yl)acetate

https://huagongshe.com/reaction/1519839

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물6-Bromoquinolin-2(1H)-oneHCID 12378943—
생성물ethyl 2-(6-bromo-2-oxoquinolin-1(2H)-yl)acetateHCID 68786198100%

반응 단계

6-Bromoquinolin-2(1H)-one (5.03 g, 22.5 mmol) was subjected to protocol K with ethyl bromoacetate instead of methyl bromoacetate to afford 6.96 g (100% yield) of ethyl 2-(6-bromo-2-oxoquinolin-1(2H)-yl)acetate as a white solid. Method [7] Retention time 4.79 min by HPLC (M+=310 and 312) and (M+Na=332 and 334). The acetate (318 mg, 1.03 mmol) was subjected to the protocol in Example 1.53.4 to afford 228 mg (83% yield) of 2-(6-bromo-2-oxoquinolin-1(2H)-yl)acetic acid as a white solid. Method [8] Retention time 4.79 min by HPLC (M+=282 and 282) and (M+Na=304 and 306).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073891B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-e4dba8e458214685b38a9255ffb3fbd9
출처 메모uspto-grants-2015_07