돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465895생성일: 2026년 10월 24일

Cystamine → 1-(2-Sulfanylethyl)pyrrolidine-2,5-dione

https://huagongshe.com/ko/reaction/465895

반응식

참여 물질

역할이름HCID투입량
반응물CystamineHCID 2915—
반응물CysteamineHCID 6058—
반응물Succinic anhydrideHCID 7922—
반응물4-Oxo-4-[(2-sulfanylethyl)amino]butanoic acidHCID 22450828—
용매WaterHCID 962—
생성물1-(2-Sulfanylethyl)pyrrolidine-2,5-dioneHCID 22016357—

반응 단계

About one-half hour is necessary for the complete transformation of the succinic anhydride (V.P.C.). At this stage, to facilitate the cyclization reaction, the reaction mixture is placed under reduced pressure and the evolution of the reaction mixture is followed by acidimetric dosage of the nontransformed N-(2-mercapto ethyl) succinamic acid. At the end of the reaction, the mixture is cooled and 7 g of crude product are obtained and dissolved in 50 cm3 of water to which are added, with stirring, 10 g of sulfonic acid resin. After stirring for one hour, the resin, having fixed the traces of cysteamine or cystamine not having reacted, is removed by filtration. To reduce the disulfide optionally present, there are added to the stirred filtrate, 10 g of sulfonic resin and 3 g of zinc powder. After 3 hours the mixture is filtered and the filtrate is concentrated under reduced pressure. After drying, 5 g of N-(2-mercapto ethyl) succinimide are obtained in the form of a white powder whose melting point is 45° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05154918
출처 데이터셋uspto-grants-1992_10
ORD IDord-9850519c0bec4d40b7c2d8c2e22ba1c0
출처 메모uspto-grants-1992_10