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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40248생성일: 2026년 10월 24일

N-Fluorobenzenesulfonimide → Methyl 2-fluoro-2-(quinolin-6-yl)acetate

https://huagongshe.com/ko/reaction/40248

반응식

참여 물질

역할이름HCID투입량
반응물N-FluorobenzenesulfonimideHCID 588007—
반응물Methyl 6-quinolineacetateHCID 1514202—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-fluoro-2-(quinolin-6-yl)acetateHCID 57691374—

반응 조건

온도-78 °C

반응 단계

To a 250 ml round-bottomed flask was added lithium bis(trimethylsilyl)amide (2.0 g, 12 mmol) and tetrahydrofuran (75 ml). The mixture was cooled to −78° C. and methyl 2-(quinolin-6-yl)acetate (2.0 g, 9.9 mmol) was added as a solution in 1 ml THF. After stirring at −78° C. for 30 min, n-fluorobenzenesulfonimide (3.8 g, 12 mmol) was added as a 1 M solution in THF. This was stirred for 30 min at −78° C. and then allowed to warm to rt. The mixture was quenched with sat NH4Cl (50 mL) and diluted with water (200 mL). The mixture was concentrated in vacuo to remove the THF and then was extracted with EtOAc (2×100 ml). The combined extracts were washed with brine (100 ml), dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (20 to 60% EtOAc/hexane) afforded the title compound as a tan solid. MS (ESI, pos. ion) m/z: 220 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8e6617c9f4714da98aa60cb1ba84aabd
출처 메모uspto-grants-2013_09