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HRID 47940Erstellt: 24. Oktober 2026

Sodium potassium tartrate tetrahydrate → 4-(3,4-Dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol

https://huagongshe.com/de/reaction/47940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium potassium tartrate tetrahydrateHCID 2724148—
EduktSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
EduktMethyl 4-(3,4-dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropionateHCID 23431809—
LösungsmittelTolueneHCID 1140—
Produkt4-(3,4-Dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanolHCID 2343180274,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Methyl 4-(3,4-dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropionate (0.67 g) was dissolved in toluene (5 mL). To the obtained solution was added dropwise a mixture of a 70% solution (0.81 g) of sodium bis(2-methoxyethoxy)aluminum hydride in toluene and toluene (2 mL) at 0° C. and the mixture was stirred at 0° C. for 1 h. To the reaction mixture was carefully added a 10% aqueous solution (50 mL) of potassium sodium (+)-tartrate tetrahydrate and the mixture was stirred at room temperature for 1 h. The precipitated crystals were collected by filtration, washed successively with a 10% aqueous solution of potassium sodium (+)-tartrate tetrahydrate, pure water and isopropyl ether, and air-dried to give the title compound as crystals (0.46 g, 74%). Recrystallization from acetone-hexane gave pale-yellow prism crystals. melting point: 140-141° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699995B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-ab8a686577f742cb8dc9fe5a54ecc8c2
Quellennotizuspto-grants-2004_03