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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40351생성일: 2026년 10월 24일

2-Methoxyethanol → Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate

https://huagongshe.com/ko/reaction/40351

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참여 물질

역할이름HCID투입량
반응물2-MethoxyethanolHCID 8019—
반응물TriphenylphosphineHCID 11776—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetateHCID 57691372—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetateHCID 5769092582%

반응 조건

온도0 °C

반응 단계

A flask was charged with tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate (581.04 mg, 2.241 mmol) and triphenylphosphine (1.175 g, 4.482 mmol) then sealed with a septum and an placed under N2. Benzene (10 mL) was added, followed by 2-methoxyethanol (0.8838 ml, 11.20 mmol). The heterogeneous solution was cooled to 0° C., and di-tert-butyl azodicarboxylate (1.032 g, 4.482 mmol) was added as a solid in a single portion. The solution was allowed to warm to rt and maintained 20 h. The solution was then partitioned between saturated aqueous. NH4Cl, and the layers separated. The aqueous layer was extracted with EtOAc (2×50 mL), and the combined organic layers were washed with brine, dried (MgSO4), and concentrated in vacuo. The resulting residue was purified by MPLC (Teledine Isco combiFlash Companion), 80 g SiO2, solvent system: 90:10 hexanes:EtOAc gradient to 50:50 hexanes:EtOAc to give tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate (585. 2 mg, 82% yield). LRMS (ESI) m/z calcd for C18H24NO4 (M+H) 318.2. found 318.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8dfdfb4c74224e3191f4dafaaac5c262
출처 메모uspto-grants-2013_09