HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 456342Erstellt: 24. Oktober 2026
Ethyl Acrylate → 1-tert-Butyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylate
https://huagongshe.com/de/reaction/456342
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | N-Boc-glycine methyl ester | HCID 637609 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-tert-Butyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylate | HCID 10868942 | — |
Reaktionsschritte
To a solution of BOC glycine methyl ester (J. Med. Chem. 2001, 44, 8, 1192-1201) (19.2 g, 101.5 mmol) in THF at 0° C. was added dropwise ethyl acrylate (11 mL, 101.5 mmol) over 10 minutes. The solution was stirred for 20 minutes, then KOtBu (111.65 mL, 111.65 mmol) was added over 45 minutes. The solution was allowed to warm to 25° C. overnight. The resulting solution concentrated in vacuo and portioned between ethyl acetate and water containing 5 mL of acetic acid. The ethyl acetate layer was removed and aqueous layer extracted with 2×200 mL of ethyl acetate. The combined ethyl acetate layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to afford an oil. MS (DCI/NH4) m/z=258 (M+H)+, 275 (M+NH4)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08497275B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-4b15624d75e04b23acafc39493a16c7c |
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| Quellennotiz | uspto-grants-2013_07 |
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