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HRID 21478Erstellt: 27. Oktober 2026
Water → N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
https://huagongshe.com/reaction/21478
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Water | HCID 962 | — |
| Edukt | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Edukt | 5-Amino-2-chloro-4-fluorophenyl methyl carbonate | HCID 10798930 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 19374481 | 79,2% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05424277 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-09cb1a08229048beaa4bbad76741f767 |
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| Quellennotiz | uspto-grants-1995_06 |
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