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HRID 490713作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromobenzoic acidHCID 11464—
反応物Sodium hydrideHCID 24758—
反応物Ammonium AcetateHCID 517165—
反応物Ethyl 2-chloro-4-methyl-3-oxopentanoateHCID 9877606—
反応物2-(4-Bromo-phenyl)4-isopropyl-oxazole-5-carboxylic acid ethyl esterHCID 69053256—
溶媒DimethylformamideHCID 6228—
生成物1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanolHCID 5876566455%

反応条件

温度90 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528160B2
出典データセットuspto-grants-2009_05
ORD IDord-7ec1f533c6a34cfba0bef15b5ed2a2fc
出典メモuspto-grants-2009_05