Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Rolziracetam | HCID 71893 | — |
| Edukt | 4-(Hydroxyimino)heptanedioic acid | HCID 20205336 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Rhodium | HCID 23948 | — |
| Produkt | 3-(5-Oxopyrrolidin-2-yl)propanoic acid | HCID 4585667 | — |
Reaktionsschritte
In a process for preparing dihydro-1H-pyrrolizine-3,5(2H, 6H)-dione comprising the steps of catalytically hydrogenating an ester of 4-(hydroxyimino)heptanedioic acid and subsequently cyclizing the resulting product to dihydro-1H-pyrrolizine-3,5(2H,6H)-dione, the improvement comprises reacting an alcoholic solution of a mono(lower alkyl) ester of 4-(hydroxyimino)heptanedioic acid, wherein lower alkyl comprises from one to three carbon atoms, with hydrogen gas at a temperature of about 60° C. in the presence of rhodium/alumina catalyst and a tertiary lower alkyl amine, wherein said lower alkyl amine comprises from three to nine carbon atoms, to produce 5-oxo-2-pyrrolidinepropanoic acid; and thereafter heating said 5-oxo-2-pyrrolidinepropanoic acid in the presence of a cyclizing agent selected from acetic anhydride, 2,2,6-trimethyl-1,3-dioxen-4-one, and diketene at a temperature of about 90° C. to produce dihydro-1H-pyrrolizine-3,5(2H,6H)-dione.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04663464 |
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| Quelldatensatz | uspto-grants-1987_05 |
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| ORD ID | ord-72f5e6ab7c96414883912fbea769defb |
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| Quellennotiz | uspto-grants-1987_05 |
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