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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490713생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromobenzoic acidHCID 11464—
반응물Sodium hydrideHCID 24758—
반응물Ammonium AcetateHCID 517165—
반응물Ethyl 2-chloro-4-methyl-3-oxopentanoateHCID 9877606—
반응물2-(4-Bromo-phenyl)4-isopropyl-oxazole-5-carboxylic acid ethyl esterHCID 69053256—
용매DimethylformamideHCID 6228—
생성물1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanolHCID 5876566455%

반응 조건

온도90 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528160B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-7ec1f533c6a34cfba0bef15b5ed2a2fc
출처 메모uspto-grants-2009_05