HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182243Erstellt: 25. Oktober 2026
Methyl morpholine oxide → 5-oxo-6-propyl-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1182243
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl morpholine oxide | HCID 82029 | — |
| Edukt | Allyl-hex-2-ynyl-carbamic acid tert-butyl ester | HCID 86600396 | — |
| Katalysator | Dicobalt Octacarbonyl (stabilized with 1-5% Hexane) | HCID 25049 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-oxo-6-propyl-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylic acid tert-butyl ester | HCID 69225356 | 38,7% |
Reaktionsschritte
A solution of allyl-hex-2-ynyl-carbamic acid tert-butyl ester (741 mg) in dichloromethane (50 mL) was added to dicobalt octacarbonyl (1.12 g) under an argon atmosphere. The resulting solution was stirred at room temperature for 1.5 h. After this time, N-methylmorpholine N-oxide (2.56 g) was added in portions during a 60 min period. Upon completion of addition, the reaction mixture was stirred for an additional 2.5 h. At the conclusion of this period, the mixture was filtered through silica gel, and the solid was washed with a 1:1 ethyl acetate-hexane solution (200 mL). The filtrate was concentrated under vacuum to yield a residue. The residue was purified by flash column chromatography to provide the title compound as a light brown oil (321 mg). MS (ES+) m/z 266.19 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07288563B2 |
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| Quelldatensatz | uspto-grants-2007_10 |
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| ORD ID | ord-e43d1ca801f642b7a7c048b3c4efd6f7 |
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| Quellennotiz | uspto-grants-2007_10 |
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