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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| 반응물 | 5-Amino-2-chloro-4-fluorophenyl methyl carbonate | HCID 10798930 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 19374481 | 79.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05424277 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-09cb1a08229048beaa4bbad76741f767 |
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| 출처 메모 | uspto-grants-1995_06 |
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