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HRID 75381作成日:2026年10月23日

Dimethyl Sulfoxide → 2-(4-Fluoro-2-nitrophenylamino)butanoic acid

https://huagongshe.com/ja/reaction/75381

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Alpha-Aminobutyric AcidHCID 6657—
反応物Potassium CarbonateHCID 11430—
反応物2,5-DifluoronitrobenzeneHCID 67767—
溶媒WaterHCID 962—
生成物2-(4-Fluoro-2-nitrophenylamino)butanoic acidHCID 19794340—

反応条件

温度80 °C

反応手順

A mixture of 2,5-difluoronitrobenzene (119 ml, 1.10 mol), 2-aminobutanoic acid (114 g, 1.10 mol), and potassium carbonate (152.2 g, 1.10 mol) in dimethyl sulfoxide (410 ml, 1.10 mol) was stirred at 80° C. for 23 h. ([Note 1]: The mixture had a deep orange red color. The internal temperature of the mixture went up to ˜110° C. for 1 h and then went down to 80° C.). After 23 h, the reaction was cooled to rt and carefully poured into water (2 L+1 L). The aqueous mixture was washed with diethyl ether (1 L×2) to remove organic impurities. The aqueous layer was then acidified to ˜pH 1.5 with concentrated HCl (300 mL) to generate a yellow solid. The yellow solid was collected by filtration, washed with water (3 L), and air-dried to give the desired product, a wet orange solid. The wet orange solid was recrystallized from 3 L toluene and stood at rt overnight to afford the desired product as an orange crystalline solid. The orange crystalline solid was filtered, washed with toluene (2 L), and dried under high vacuum at 80° C. for 4 h and then on lyophilizer overnight to afford 2-(4-fluoro-2-nitrophenylamino)-butanoic acid (203.6 g, 76.4% yield) as an orange crystalline solid. The orange crystalline solid was carried on without further purification to the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835432B2
出典データセットuspto-grants-2014_09
ORD IDord-789d4e02666c467a83595a3c1a9c6fcb
出典メモuspto-grants-2014_09