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HRID 128684作成日:2026年10月26日

3-Phenoxybenzoic acid → 5-Acetyl-4-methyl-2-(3-phenoxyphenyl)oxazole

https://huagongshe.com/reaction/128684

反応式

関与物質

役割名称HCID仕込み量
反応物3-Phenoxybenzoic acidHCID 19539—
反応物3-PhenoxybenzamideHCID 16618625—
溶媒Sodium HydroxideHCID 14798—
生成物5-Acetyl-4-methyl-2-(3-phenoxyphenyl)oxazoleHCID 1937492894%

反応条件

温度180 °C

反応手順

A mixture of 3-phenoxybenzamide (2.13 g, 10 mmol), 3-phenoxybenzoic acid (4.28 g, 20 mmol), and 3-chloropenta-2,4-dione (0.44 g, 3.3 mmol) was heated to 180° C. under stirring for 23 h. The hot mixture was poured into 1N aqueous sodium hydroxide (100 ml), and extracted with diethyl ether (100+2×50 ml). The combined organic phases were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml), dried over magnesium sulfate, and evaporated to dryness. Purification by silica gel column chromatography (135 g, 16.7% ethyl acetate in n-hexane) afforded the titled compound as solids in 94% yield: 1H NMR (CDCl3) δ7.88-7.83 (1H, m), 7.77-7.53 (1H, m), 7.49-7.34 (3H, m), 7.18-7.12 (2H, m), 7.07-7.00 (2H, m), 2.55 (3H, s), 2.54 (3 H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464849
出典データセットuspto-grants-1995_11
ORD IDord-73a8b1f0a08048a8937510601d49b623
出典メモuspto-grants-1995_11