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HRID 128534생성일: 2026년 10월 26일
Bromocyclopentane → N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
https://huagongshe.com/reaction/128534
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromocyclopentane | HCID 8728 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1H-Isoindole-1,3(2H)-dione, 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-4,5,6,7-tetrahydro- | HCID 158651 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 15279390 | 30.5% |
반응 단계
Cyclopentyl bromide (1.2 g, 8.1 mmol) was added to a solution of N-(2-fluoro-4-chloro-5-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide (2.0 g, 6.76 mmol) and potassium carbonate (0.60 g, 4.34 mmol) in acetonitrile (50 ml), followed by stirring for 2 hours under refluxing. After completion of the reaction, IN hydrochloric acid (20 ml) was added to the resulting reaction mixture, and the mixture was extracted with ethyl acetate (20 ml×3 times). The organic layer was washed with water, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Ethanol (5 ml) was added to the resulting pale yellow oily substance, and the precipitated N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide as a white solid (0.75 g, 2.06 mmol, 30.5% yield) was isolated by filtration. Spectral data and the like are as shown in Example 1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05464811 |
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| 출처 데이터셋 | uspto-grants-1995_11 |
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| ORD ID | ord-8e55d0c2361449abaebdb674398956ad |
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| 출처 메모 | uspto-grants-1995_11 |
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