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HRID 267080作成日:2026年10月27日

Ethyl Acetate → 1-(4-Nitrophenylmethyl)-1H-imidazol-5-ylacetic acid methyl ester

https://huagongshe.com/reaction/267080

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物4-Nitrobenzyl bromideHCID 66011—
反応物1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl esterHCID 10523967—
溶媒AcetonitrileHCID 6342—
生成物1-(4-Nitrophenylmethyl)-1H-imidazol-5-ylacetic acid methyl esterHCID 70180988—

反応条件

温度55 °C

反応手順

To a solution of 1-(triphenylmethyl)-1H-imidazol-4-ylacetic acid methyl ester (23, 274 mg, 0.736 mmol) in acetonitrile (10 ml) was added 4-nitrobenzylbromide (159 mg, 0.736 mmol) and heated to 55° C. for 16 h. After this time, the reaction was cooled to room temperature, treated with ethyl acetate (20 ml) and the resulting precipitate was filtered. The filtrate was concentrated to dryness in vacuo and the residue was redissolved in acetonitrile (4 ml) and heated to 65° C. for 3 h. After this time, the reaction mixture was evaporated to dryness and combined with initial precipitate. This residue was dissolved in methanol (5 ml) and heated to reflux for 30 min. The resulting solution was evaporated in vacuo and the residue was purified by flash chromatography (2-5% methanol/methylene chloride gradient elution) to provide 16.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652257
出典データセットuspto-grants-1997_07
ORD IDord-3fc800d25cf44c47acb266e7f13f3efd
出典メモuspto-grants-1997_07