戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 30657作成日:2026年10月24日

Dimethylformamide → 4-Methyl-2-(4-nitrobenzyl)-1,3-oxazole

https://huagongshe.com/ja/reaction/30657

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物BromoacetoneHCID 11715—
反応物2-(4-Nitrophenyl)acetamideHCID 233613—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-Methyl-2-(4-nitrobenzyl)-1,3-oxazoleHCID 203924868.3%

反応条件

温度120 °C

反応手順

A mixture of 2-(4-nitrophenyl)acetamide (15.0 g), 1-bromo-2-propanone (19.03 g), and N,N-dimethylformamide (2 mL) was stirred at 120° C. for 3 hrs. Water, potassium carbonate and ethyl acetate were added to basify the reaction mixture and the mixture was extracted with ethyl acetate. Insoluble materials were filtered off, and the organic layer was separated. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 4-methyl-2-(4-nitrobenzyl)-1,3-oxazole as orange crystals (1.50 g, yield 8.2%) from a fraction eluted with hexane-ethyl acetate (2:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 67-68° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-40f0570cae5c4f9faf01964bbeb1d0b6
出典メモuspto-grants-2008_09