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HRID 485270作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物S-benzyl-L-cysteineHCID 193613—
反応物Sodium BicarbonateHCID 516892—
反応物N-(Methoxycarbonyl)maleimideHCID 580610—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Chloroform ethyl acetate acetic acidHCID 87343015—
生成物(2S)-3-benzylthio-2-maleimidopropionic acidHCID 1349034719.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04536391
出典データセットuspto-grants-1985_08
ORD IDord-4796f2babb304a589c11dfce2f572d94
出典メモuspto-grants-1985_08