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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276111생성일: 2026년 10월 24일

Cesium carbonate → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester

https://huagongshe.com/ko/reaction/276111

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-Methoxy-alpha-toluenethiolHCID 80407—
반응물Ethyl acetate hexaneHCID 21226206—
반응물2-bromopentanoyl-(L)-homophenylalanine methyl esterHCID 22950831—
촉매Tetrabutylammonium IodideHCID 67553—
용매DimethylformamideHCID 6228—
생성물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl esterHCID 22950828—

반응 단계

Combine 2-bromopentanoyl-(L)-homophenylalanine methyl ester (3.6 g, 10 mmol), 4-methyoxybenzylmercaptan (3.48 mL, 25 mmol), and tetrabutylammonium iodide (about 50 mg) in dimethylformamide (10 mL). Degas by repeatedly applying vacuum and filling the vessel with nitrogen. Add cesium carbonate (4.10 g, 12.5 mmol). After 15 hours, partition the reaction mixture between water and methyl t-butyl ether, saturate the aqueous layer with sodium chloride. Extract the aqueous layer with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 4/1 hexane/ethyl acetate and then 2.5/1 hexane/ethyl acetate to give the title compound: Rf=0.44 (silica gel, 2.5/1 hexane/ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352976B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-d1385ca9dc824c218ae0cd8094c64e04
출처 메모uspto-grants-2002_03