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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3116생성일: 2026년 10월 23일

Water → Dimethyl 7-chloroquinoline-2,3-dicarboxylate

https://huagongshe.com/ko/reaction/3116

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium FormateHCID 2723810—
반응물Dimethyl 4,7-dichloroquinoline-2,3-dicarboxylateHCID 18929951—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물Dimethyl 7-chloroquinoline-2,3-dicarboxylateHCID 18929843134.8%

반응 단계

A stirred mixture of dimethyl 4,7-dichloroquinoline-2,3-dicarboxylate (5.00 g, 15.9 mM), sodium formate (1.63 g, 23.9 mM) and tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) in anhydrous dimethylformamide (75 mL) under a nitrogen atmosphere was heated at 90°-95° C. for 7 hr. No reaction occurred so the reaction mixture was degassed and an additional quantity of tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) was added and the reaction mixture again heated at 90°-95° C. for 6 hr. The cooled reaction mixture was poured into water and the resulting mixture extracted with ethyl acetate. The combined extracts were dried (MgSO4), filtered and concentrated to leave an gummy solid (6.0 g). Trituration of this residue with ethyl acetate and subsequent filtration separated a crystalline solid which was shown to be dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate. The filtrate was concentrated and the residue was flash chromatographed over silica gel (eluant: hexane/ethyl acetate, 3/2) to provide the title diester (1.13 g, 25.4%) as a light yellow crystalline solid; MS(CI): 280 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733910
출처 데이터셋uspto-grants-1998_03
ORD IDord-e1f559619b474a8e8ddc858df147e65a
출처 메모uspto-grants-1998_03