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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276114생성일: 2026년 10월 23일

Carbon Tetrachloride → 2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine

https://huagongshe.com/ko/reaction/276114

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물AnisoleHCID 7519—
반응물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl esterHCID 54481559—
촉매Mercuric acetateHCID 15337—
용매DichloromethaneHCID 6344—
생성물2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanineHCID 1554874058.2%

반응 단계

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine t-butyl ester (0.20 g, 0.33 mmol), mercury (II) acetate (0.134 g, 0.42 mmol), and anisole (0.37 mL, 3.4 mmol) in dichloromethane (9 mL). Cool in an ice bath and degas by repeatedly applying vacuum and filling the vessel with nitrogen, Add trifluoroacetic acid (4 mL). After 1 hour, warm to ambient temperature. After 3 hours, purge with hydrogen sulfide (gas) for about 10 minutes. Filter and evaporate in vacuo to give a residue. Repeatedly, combine the residue and carbon tetrachloride and evaporate in vacuo to give a residue. Triturate the residue with hexane to give the title compound as a solid (85 mg, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352976B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-5ae5529245274703a3c1f8b6e322927e
출처 메모uspto-grants-2002_03