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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47931Erstellt: 24. Oktober 2026

O-Cresol → 4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole

https://huagongshe.com/de/reaction/47931

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-CresolHCID 335—
EduktSodium HydroxideHCID 14798—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanolHCID 9926997—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelTriethylamineHCID 8471—
Produkt4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 988767291,2%

Reaktionsschritte

To a solution of 4-(4-chlorophenyl)-5-(3-hydroxypropyl)-2-(2-methylimidazol-1-yl)oxazole (509 g), triethylamine (254.6 mL) in toluene (4072 mL) was added dropwise methanesulfonyl chloride (136.4 mL) at not higher than 10° C. Ten minutes later, o-cresol (248.0 mL) and tetrabutylammonium bromide (25.8 g) were added to the obtained mixture and a solution of NaOH (255 g) in water (1018 mL) was further added. The mixture was heated under reflux for 1 h. After cooling, the toluene layer was separated and washed with 1N aqueous NaOH solution (4072 mL×3) and then with 5% aqueous NaCl solution. The solvent was evaporated and the obtained crystals were recrystallized from ethanol-water (9:1) to give the title compound (595.6 g, yield: 91.2%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699995B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-8c6af652983a4487ad552939860ff0e2
Quellennotizuspto-grants-2004_03