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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1703983Erstellt: 25. Oktober 2026

p-Toluenesulfonic acid → 3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dione

https://huagongshe.com/reaction/1703983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktPotassium HydroxideHCID 14797—
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
Edukt1,1,3,3-TetramethylguanidineHCID 66460—
EduktDiisopropylethylamineHCID 81531—
EduktBarium Oxide Nanoparticle DispersionHCID 9855530—
EduktTetramethylbenzyl ammonium hydroxideHCID 19860286—
Produkt3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dioneHCID 2729247—

Reaktionsschritte

The above procedure is repeated in all respects, excepting that the strong base reagent is altered, In separate experiments, sodium hydride, potassium hydroxide, barium oxide, diisopropylethylamine, 1,5-diazobicylo[5.4.0]undicene5, tetramethylguanidine, tetramethylbenzyl ammonium hydroxide, Amberlite A21 (Rohm & Haas) strongly basic ion exchange resin or p-toluene sulfonic acid, are substituted for sodium hydroxide and yield the desired 3-isopropyl-3-methyl-5H-imidazo[2,1-a]isoindole-2(3H),5-dione. In practice of the above-described method, sodium hydroxide or sodium hydride in refluxing toluene is preferred.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04125727
Quelldatensatzuspto-grants-1978_11
ORD IDord-c14705e1a1124e52b08757da855bc58d
Quellennotizuspto-grants-1978_11