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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl morpholine oxideHCID 82029—
EduktAllyl-hex-2-ynyl-carbamic acid tert-butyl esterHCID 86600396—
KatalysatorDicobalt Octacarbonyl (stabilized with 1-5% Hexane)HCID 25049—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-oxo-6-propyl-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylic acid tert-butyl esterHCID 6922535638,7%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07288563B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-e43d1ca801f642b7a7c048b3c4efd6f7
Quellennotizuspto-grants-2007_10