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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36922생성일: 2026년 10월 24일

Oxalyl chloride → 2,4-Difluorophenylacetyl chloride

https://huagongshe.com/ko/reaction/36922

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물2,4-Difluorophenylacetic acidHCID 123581—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물2,4-Difluorophenylacetyl chlorideHCID 15231606—

반응 단계

To a mixture of 2,4-difluorophenylacetic acid (206 mg), DMF (1 drop) and tetrahydrofuran (4 ml) was added oxalyl chloride (0.13 ml) dropwise. The resulting mixture was stirred at room temperature for 1 hour and the solvent was then distilled off to give 2,4-difluorophenylacetyl chloride. This chloride was dissolved in dichloromethane (5 ml) followed by addition of 3-amino-4-(2-chlorophenyl)-7,8-dihydro-6H-cyclopenta[g]quinoline (294 mg) and N,N-dimethylaniline (0.13 ml). The mixture was further stirred at room temperature for 3 hours, after which it was washed with water, saturated aqueous solution of NaHCO3 and water in the order mentioned and dried (over MgSO4). The solvent was then distilled off to give 4-(2-chlorophenyl)-3-(2,4-difluorophenylacetylamino)-7,8-dihydro-6H-cyclopenta(g)quinoline as oil. This oil was crystallized from isopropyl ether (yield 342 mg, 76.3%). Recrystallization from ethanol gave colorless prisms, mp. 179°-180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05418239
출처 데이터셋uspto-grants-1995_05
ORD IDord-7136b0aec2a94decbecda8f435272e8f
출처 메모uspto-grants-1995_05