HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20747Erstellt: 23. Oktober 2026
N-Hydroxyphthalimide → Ethyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoate
https://huagongshe.com/de/reaction/20747
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 4-((1,3-dioxoisoindolin-2-yl)oxy)butanoate | HCID 10850119 | 100% |
Reaktionsschritte
To a solution of 4-bromo-n-butyric acid ethyl ester (1.2 g, 6.13 mmol) in dimethylformamide (9 ml) were added N-hydroxyphthalimide (1.5 g, 9.19 mmol) and Hunig base (N,N-diisopropylethylamine, 2.13 mL) at room temperature, and the mixture was stirred at 80° C. over night. The reaction mixture was poured into saturated aqueous ammonium chloride, and the resultant mixture was extracted with ethyl acetate (3×40 ml). The combined organic layers were washed with saturated brine (2×30 ml), dried over Na2SO4, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (100 g, n-hexane/ethyl acetate (2:1)) to give 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester (1.47 g, 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745663B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-3f4a91da137348fab27f70c6fd15f396 |
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| Quellennotiz | uspto-grants-2010_06 |
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