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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40182생성일: 2026년 10월 24일

Tetrahydrofuran → Ethyl 3-(7-methoxyquinolin-4-yl)propanoate

https://huagongshe.com/ko/reaction/40182

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
반응물4-Chloro-7-methoxyquinolineHCID 10607829—
반응물HCID 178471816HCID 178471816—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Ammonium HydroxideHCID 14923—
생성물Ethyl 3-(7-methoxyquinolin-4-yl)propanoateHCID 67503802—

반응 단계

4-chloro-7-methoxyquinoline (0.35 g, 2 mmol), tri-t-butylphosphonium tetrafluoroborate (0.05 g, 0.2 mmol), and tris(dibenzylideneacetone)dipalladium (0) (0.08 g, 0.09 mmol) were combined. The reaction vessel was purged and flushed with nitrogen three times, followed by addition of 3-ethoxy-3-oxopropylzinc bromide in THF (10 mL, 5 mmol, 0.5 M). The reaction mixture was microwaved at 150° C. for 60 minutes. Upon completion, ammonium hydroxide (10 mL) was added. After 30 minutes the mixture was filtered and the filtrate was partitioned between water and ethyl acetate. Extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated. Purified by MPLC with a gradient of 20 to 50% EtOAc in CH2Cl2. (ESI, pos. ion) m/z: 354.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2749dc371527437e9924f4eb2acea80b
출처 메모uspto-grants-2013_09