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HRID 257640作成日:2026年10月26日

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

https://huagongshe.com/reaction/257640

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Hydroxyphenyl)propionic acidHCID 10394—
反応物2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
反応物Ammonium AcetateHCID 517165—
反応物SodiumHCID 5360545—
触媒Sulfuric AcidHCID 1118—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物4-[2-(4,5-Diphenyl-2-oxazolyl)ethyl]phenolHCID 1978362365.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262540
出典データセットuspto-grants-1993_11
ORD IDord-5ed5493abe86493caa1b6c377111fbeb
出典メモuspto-grants-1993_11