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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1637152Erstellt: 24. Oktober 2026

Dimethadione → 2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisole

https://huagongshe.com/de/reaction/1637152

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethadioneHCID 3081—
EduktPotassium CarbonateHCID 11430—
Edukt2-[3-(1-Adamantyl)-2-chloro-3-oxopropanamido]-4-nitroanisoleHCID 19347758—
LösungsmittelAcetoneHCID 180—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisoleHCID 5387966679,8%

Reaktionsschritte

A suspension of 16.28 g (0.04 mol) of [4], 5.17 g (0.04 mol) of 5,5-dimethyloxazolidine-2,4-dione, and 16.58 g (0.12) mol of anhydrous potassium carbonate in 380 mL of dried acetone was refluxed for 3 hours. Thin layer chromatographic analysis indicated that the reaction was complete. The reaction mixture was concentrated in vacuo to yield an orange-colored solid. It was dissolved in ethyl acetate and the organic layer was washed with HCl (10%) and brine until neutrality. The organic layer was dried, filtered, and concentrated to yield an oil which solidified upon standing. It was triturated in ligroin. The final dried product (15.92 g, 79.8%) gave one spot on TLC. All analytical data confirmed the assigned structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06040126
Quelldatensatzuspto-grants-2000_03
ORD IDord-8147e9c6089444d39b250676fc062f57
Quellennotizuspto-grants-2000_03