HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550788Erstellt: 25. Oktober 2026
Diethyl Malonate → Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate
https://huagongshe.com/reaction/550788
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diethyl Malonate | HCID 7761 | — |
| Edukt | Ethanol sodium ethoxide | HCID 23706232 | — |
| Edukt | 1-Tert-butoxycarbonylpiperidin-4-yl benzenesulfonate | HCID 86619135 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate | HCID 59605280 | — |
Reaktionsschritte
A mixture of 1-tert-butoxycarbonylpiperidin-4-ol, triethylamine, benzenesulfonyl chloride, and methylene chloride was stirred at ambient temperature for 2 days to yield 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate. A mixture of 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate obtained, diethyl malonate, 20% NaOEt-EtOH, and EtOH was heated under reflux with stirring for 22 hours to yield diethyl[1-(tert-butoxycarbonyl)piperidin-4-yl]malonate. A mixture of diethyl [1-(tert-butoxycarbonyl)piperidin-4-yl]malonate obtained, lithium borohydride, toluene, and THF was stirred at 60° C. for 18 hours to yield 2-(1-tert-butoxycarbonylpiperidin-4-yl)propane-1,3-diol, which was stirred together with 4M HCl-dioxane solution in MeOH at ambient temperature for 1 hour to yield 2-piperidin-4-ylpropane-1,3-diol hydrochloride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07947690B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-2ea39f6b43514390b30e9904b0204f6a |
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| Quellennotiz | uspto-grants-2011_05 |
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