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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75381생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Alpha-Aminobutyric AcidHCID 6657—
반응물Potassium CarbonateHCID 11430—
반응물2,5-DifluoronitrobenzeneHCID 67767—
용매WaterHCID 962—
생성물2-(4-Fluoro-2-nitrophenylamino)butanoic acidHCID 19794340—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835432B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-789d4e02666c467a83595a3c1a9c6fcb
출처 메모uspto-grants-2014_09