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HRID 28597作成日:2026年10月26日

Triphenylphosphine → 3-[5-(4-Nitro-phenyl)-oxazol-2-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/28597

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Butanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
反応物2-Azido-1-(4-nitrophenyl)ethanoneHCID 16749257—
溶媒1,2-DichloroethaneHCID 11—
生成物3-[5-(4-Nitro-phenyl)-oxazol-2-yl]-propionic acid methyl esterHCID 6898750623%

反応条件

温度85 °C

反応手順

To a mixture of crude 2-azido-1-(4-nitrophenyl)-ethanone (8.2 mmol) and 1,2,-dichloroethane (80 ml) was added 3-chlorocarbonyl-propionic acid methyl ester (1.1 ml, 9.0 mmol) and triphenylphosphine (2.4 g, 9.0 mmol). The mixture was stirred at 85° C. for 12 hours. After cooling to room temperature, the mixture was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4 followed by 1:1) to give 3-[5-(4-nitro-phenyl)-oxazol-2-yl]-propionic acid methyl ester (520 mg, 23% yield for 2 steps). 1H NMR (acetone-d6) δ 2.92 (t, 2H, J=7.1 Hz, CH2), 3.19 (t, 2H, J=7.1 Hz, CH2), 3.68 (s, 3H, CH3), 7.74 (s, 1H, Ar), 7.98 (d, 2H, J=9.0 Hz, Ar), 8.34 (d, 2H, J=9.0 Hz, Ar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-87d8e9df26614fe39c0741c0cb71f2ce
出典メモuspto-grants-2008_09