Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Butyl chloroformate | HCID 61140 | — |
| Edukt | 2-(2-Oxopyrrolidin-1-yl)acetic acid | HCID 3146687 | — |
| Edukt | HCID 21279295 | HCID 21279295 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 20163719 | HCID 20163719 | — |
Reaktionsschritte
An ice cold solution of 2-oxo-1-pyrrolidineacetic acid (2.2 g) and triethylamine (2.15 ml) in dimethylformamide (10 ml) was treated dropwise while stirring with butyl chloroformate (1.95 ml). After stirring at 0° C. for 30 minutes, 2,2-dimethyl-4-imidazolidinone (1.75 g) was added at once, and stirring was continued at room temperature overnight. After evaporation under reduced pressure the residue was chromatographed on a silica gel column, eluting with dichloromethane/methanol 1:1. The selected fractions were collected and evaporated to give an oil which was washed twice with ethyl acetate. The residue was crystallized from ethyl acetate, to give the title compound as a white powder, m.p. 214°-217° C. (decomp.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04703054 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-45569acc942d413f8c9274721a09a574 |
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| Quellennotiz | uspto-grants-1987_10 |
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