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HRID 485270Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktS-benzyl-L-cysteineHCID 193613—
EduktSodium BicarbonateHCID 516892—
EduktN-(Methoxycarbonyl)maleimideHCID 580610—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelChloroform ethyl acetate acetic acidHCID 87343015—
Produkt(2S)-3-benzylthio-2-maleimidopropionic acidHCID 1349034719,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04536391
Quelldatensatzuspto-grants-1985_08
ORD IDord-4796f2babb304a589c11dfce2f572d94
Quellennotizuspto-grants-1985_08