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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 366538Erstellt: 26. Oktober 2026

Dimethylformamide → 3-(3-Methylbut-1-y)-3-azabicyclo[3.1 .0]hexane-2,4-dione

https://huagongshe.com/reaction/366538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1-Iodo-3-methylbutaneHCID 10924—
EduktSodium hydrideHCID 24758—
Edukt3-Azabicyclo[3.1.0]hexane-2,4-dioneHCID 3720053—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3-Methylbut-1-y)-3-azabicyclo[3.1 .0]hexane-2,4-dioneHCID 70106366—

Reaktionsschritte

Sodium hydride (0.11 g) was added to a solution of 3-azabicyclo[3.1.0]hexane-2,4-dione (0.3 g) in dry tetrahydrofuran (10 ml) under a nitrogen atmosphere at room temperature. The suspension was stirred for 5 minutes and 1-iodo-3-methylbutane (0.53 g) was then added in one portion to the reaction mixture. After stirring for two hours at room temperature, dimethylformamide (5 ml) was added and the reaction mixture was stirred for a further 16 hours at room temperature. The reaction mixture was diluted with dichloromethane and then partitioned with water (20 ml). The aqueous phase was extracted with dichloromethane (20 ml) and the combined organic extracts were washed with water (2×20 ml), dried (MgSO4) and evaporated in vacuo. The residue was purified by chromatography on silica gel (50 g) using 25% ethyl acetate/hexane as eluant to give the title compound as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06130241
Quelldatensatzuspto-grants-2000_10
ORD IDord-f67b1f97e3304ec4b9d50edb85072123
Quellennotizuspto-grants-2000_10