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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490713Erstellt: 24. Oktober 2026

4-Bromobenzoic acid → 1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanol

https://huagongshe.com/de/reaction/490713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromobenzoic acidHCID 11464—
EduktSodium hydrideHCID 24758—
EduktAmmonium AcetateHCID 517165—
EduktEthyl 2-chloro-4-methyl-3-oxopentanoateHCID 9877606—
Edukt2-(4-Bromo-phenyl)4-isopropyl-oxazole-5-carboxylic acid ethyl esterHCID 69053256—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanolHCID 5876566455%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

2-(4-Bromo-phenyl)-4-isopropyl-oxazole-5-carboxylic acid ethyl ester A solution of 4-bromo-benzoic acid (34.0 g, 0.169 mol) in DMF (450 mL) is treated at ambient temperature portionwise with NaH (6.4 g, 0.16 mol, 60% oil dispersion). The suspension is heated to 90° C. and 2-chloro-4-methyl-3-oxo-pentanoic acid ethyl ester (27.7 g, 0.144 mol) is added neat. The remaining chloride is washed into the reaction flask using DMF (25 mL). The reaction mixture is stirred for 18 h, cooled, and treated with water (600 mL). The mixture is extracted with EtOAc (750 mL). The organic layer is washed with brine (2×250 mL), dried (Na2SO4), and concentrated to a foam (56 g). This diester is dissolved in acetic acid (500 mL), treated at ambient temperature with ammonium acetate (80 g, 1.0 mol), and heated at 120° C. for 20 h. The reaction mixture is cooled, concentrated, and partitioned between EtOAc (500 mL) and saturated NaHCO3 solution (3×125 mL). The organic layer is dried (Na2SO4), and concentrated. The crude product is purified by silica gel flash chromatography using hexanes:ethyl acetate (6:1) to give the title compound (26.6 g, 55%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528160B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-7ec1f533c6a34cfba0bef15b5ed2a2fc
Quellennotizuspto-grants-2009_05