HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602164Erstellt: 24. Oktober 2026
Phthalimide → N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimide
https://huagongshe.com/de/reaction/602164
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phthalimide | HCID 6809 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate | HCID 58992598 | — |
| Edukt | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimide | HCID 58992691 | 95% |
Reaktionsschritte
Triphenylphosphine (1.68 g, 6.20 mmol) and phthalimide (799 mg, 5.43 mmol) were added to methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate (1.29 g, 5.17 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 10 min and a 40% diethyl azodicarboxylate/toluene solution (3.52 mL, 7.76 mmol) was added. The mixture was then stirred at room temperature for 8 hours. Subsequently, water was added and the mixture was extracted with ethylacetate. The extract was washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=20:1->5:1) gave 1.85 g (95%) of the desired compound as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07902367B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-0cc93c605ff844d78e7a84d99a0d7f4f |
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| Quellennotiz | uspto-grants-2011_03 |
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