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HRID 257640생성일: 2026년 10월 24일

3-(4-Hydroxyphenyl)propionic acid → 4-[2-(4,5-Diphenyl-2-oxazolyl)ethyl]phenol

https://huagongshe.com/ko/reaction/257640

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Hydroxyphenyl)propionic acidHCID 10394—
반응물2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
반응물Ammonium AcetateHCID 517165—
반응물SodiumHCID 5360545—
촉매Sulfuric AcidHCID 1118—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물4-[2-(4,5-Diphenyl-2-oxazolyl)ethyl]phenolHCID 1978362365.1%

반응 단계

Sodium metal (1.00 g, 43 mg atom) was dissolved in ethanol (125 mL) and 3-(4-hydroxyphenyl)propionic acid (6.04 g, 36 mmol) added to give a white precipitate. The mixture was warmed briefly with stirring and concentrated H2SO4 (3 drops) added followed by 2-bromo-2-phenylacetophenone (1.00 g, 36 mmol). The mixture was heated at reflux for 2 hours, cooled, concentrated and diluted with water. The mixture was extracted with CH2Cl2, the combined extracts dried over sodium sulfate and concentrated to give an oil which was dissolved in acetic acid (250 mL). Ammonium acetate (14.00 g, 180 mmol) was added and the mixture heated to reflux. After 100 minutes, the solution was cooled, diluted with water and extracted with CH2Cl2. The combined extracts were dried over sodium sulfate and the solvent evaporated to leave a solid that was triturated with a mixture of hexanes and diethyl ether and filtered to give 4-[2 -(4,5-diphenyl-2-oxazolyl)ethyl]phenol (8.00 g, 64%). An analytical sample was prepared by recrystallizing 1.5 g from a mixture of hexanes and CH2Cl2 to give 1.20 g of pure material, m.p. 142°-144° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262540
출처 데이터셋uspto-grants-1993_11
ORD IDord-5ed5493abe86493caa1b6c377111fbeb
출처 메모uspto-grants-1993_11