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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485270생성일: 2026년 10월 24일

Sulfuric Acid → (2S)-3-benzylthio-2-maleimidopropionic acid

https://huagongshe.com/ko/reaction/485270

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물S-benzyl-L-cysteineHCID 193613—
반응물Sodium BicarbonateHCID 516892—
반응물N-(Methoxycarbonyl)maleimideHCID 580610—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Chloroform ethyl acetate acetic acidHCID 87343015—
생성물(2S)-3-benzylthio-2-maleimidopropionic acidHCID 1349034719.7%

반응 단계

According to the method of O. Keller and J. Rudinger (Helv. Chim. Acta., 58, 531 (1975)), 6.2 g (40 mmols) of N-methoxycarbonylmaleimide was added at 0° C. to a solution of 8.44 g (40 mmols)of S-benzyl-L-cysteine in a mixture of 200 ml of saturated aqueous solution of sodium hydrogen carbonate and 100 ml of THF. The mixture was stirred for 10 minutes and then diluted with 300 ml of water and 150 ml of THF. The reaction mixture was stirred at room temperature for 30 minutes and subsequently at 40° C. for 30 minutes, neutralized with concentrated sulfuric acid and thereafter concentrated to about 200 ml in a vacuum. The concentrate was subjected to extraction with ethyl acetate, and the extract was dried over anhydrous sodium sulfate (Na2SO4) and concentrated to give a white solid. The product was subjected to silica gel chromatography (90:10:5 chloroform-ethyl acetate-acetic acid to 40:60:5 chloroform-ethyl acetate-acetic acid), giving 2.29 g of (2S)-3-benzylthio-2-maleimidopropionic acid. M.p.: 86°-87° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04536391
출처 데이터셋uspto-grants-1985_08
ORD IDord-4796f2babb304a589c11dfce2f572d94
출처 메모uspto-grants-1985_08