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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 519621Erstellt: 24. Oktober 2026

3-Ethoxy-2-methyl-3-oxopropane-1-diazonium → HCID 178438641, Verbindung

https://huagongshe.com/de/reaction/519621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Ethoxy-2-methyl-3-oxopropane-1-diazoniumHCID 86644035—
EduktHCID 178438592HCID 178438592—
KatalysatorHCID 178476747HCID 178476747—
LösungsmittelTolueneHCID 1140—
ProduktHCID 178438641HCID 17843864189%

Reaktionsschritte

To a mixture of 4′-{[4-(trans-4-hydroxycyclohexyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (4 g), rhodium(I) acetate (0.028 g) and toluene (70 mL) was added dropwise a solution (10 mL) of 3-ethoxy-2-methyl-3-oxopropane-1-diazonium (5.5 mL) in toluene at 80° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was concentrated, and the obtained residue was purified by silica gel column chromatography. The obtained residue was dissolved in tetrahydrofuran (20 mL) and methanol (20 mL), and 1N aqueous sodium hydroxide solution (20 mL) was added. The reaction mixture was stirred for 1 hr, 1N aqueous hydrochloric acid solution was added, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (4.1 g, 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115136B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-1a9e26cb03544b168892c6f25fdac07f
Quellennotizuspto-grants-2015_08