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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21478생성일: 2026년 10월 25일

Water → N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide

https://huagongshe.com/reaction/21478

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
반응물5-Amino-2-chloro-4-fluorophenyl methyl carbonateHCID 10798930—
용매Acetic AcidHCID 176—
생성물N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimideHCID 1937448179.2%

반응 단계

A solution of 2-fluoro-4-chloro-5-methoxycarbonyloxyaniline (20.0 g, 91.1 mmol) and 3,4,5,6-tetrahydrophthalic anhydride (14.0 g, 92.0 mmol) in acetic acid (200 ml) was reacted for 5 hours while heating under refluxing. After completion of the reaction, the mixture was-cooled to room temperature, water (200 ml) was added thereto, and extracted with ethyl acetate (100 ml×3 times). The organic layer was washed with an aqueous solution of sodium carbonate and water, dried, and the solvent was distilled off under reduced pressure. The resulting oily substance was purified by silica gel column chromatography (development solvent: ethyl acetate/hexane=1/5) to obtain N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide as a white solid (26.2 g, 72.1 mmol, 79.2% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424277
출처 데이터셋uspto-grants-1995_06
ORD IDord-09cb1a08229048beaa4bbad76741f767
출처 메모uspto-grants-1995_06