HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 354065Erstellt: 23. Oktober 2026
Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → (1-Benzylpyrrolidin-3-yl)methanol
https://huagongshe.com/de/reaction/354065
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate | HCID 98909 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | (1-Benzylpyrrolidin-3-yl)methanol | HCID 5176654 | — |
Reaktionsschritte
First, N-benzyl-pyrrolidine-3-methanol was prepared as follows. Methyl N-benzyl-5-oxo-pyrrolidine-3-carboxylate (11.66 g, 50 mmol) was dissolved in diethyl ether and cooled to 0° C. This solution was added to a 0° C. suspension of lithium aluminum hydride in diethyl ether under nitrogen atmosphere. After addition, the mixture was refluxed for 1 hr, and then cooled with an ice bath. To quench the reaction, sodium sulfate decahydrate was added and the mixture was stirred for 1 hr. After filtration, the filtrate was collected, and concentrated to dryness to give N-Benzyl-pyrrolidine-3-methanol. ESMS (C12H17NO): calcd. 191.13; obsd. 192.2 [M+H]+. Retention time (anal. HPLC: 10-70% MeCN/H2O over 5 min)=0.95 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06756400B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-10446a06760146dab4d29bc9145fdae5 |
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| Quellennotiz | uspto-grants-2004_06 |
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