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HRID 276111作成日:2026年10月26日

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

https://huagongshe.com/reaction/276111

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-Methoxy-alpha-toluenethiolHCID 80407—
反応物Ethyl acetate hexaneHCID 21226206—
反応物2-bromopentanoyl-(L)-homophenylalanine methyl esterHCID 22950831—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒DimethylformamideHCID 6228—
生成物2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl esterHCID 22950828—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352976B1
出典データセットuspto-grants-2002_03
ORD IDord-d1385ca9dc824c218ae0cd8094c64e04
出典メモuspto-grants-2002_03