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HRID 1064881作成日:2026年10月26日

Potassium Iodide → (S)-2-Ethoxy-3-[2-methyl-4-(5-methyl-2-o-tolyl-oxazol-4-ylmethoxy)-phenyl]-propionic acid methyl ester

https://huagongshe.com/reaction/1064881

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Cesium carbonateHCID 10796—
反応物4-(Chloromethyl)-5-methyl-2-(2-methylphenyl)-1,3-oxazoleHCID 21974258—
反応物(S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionic acid methyl esterHCID 68616579—
溶媒AcetoneHCID 180—
生成物(S)-2-Ethoxy-3-[2-methyl-4-(5-methyl-2-o-tolyl-oxazol-4-ylmethoxy)-phenyl]-propionic acid methyl esterHCID 6928046270.6%

反応手順

A mixture of (S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionic acid methyl ester (80 mg, 0.34 mmol), 4-chloromethyl-5-methyl-2-o-tolyl-oxazole (82 mg, 0.37 mmol), cesium carbonate (120 mg, 0.37 mmol) and a trace of potassium iodide were suspended in acetone (8 ml). The suspension was heated under reflux for 5 h, the solvent evaporated under reduced pressure and the residue dissolved in 2 N HCl/ice water 1/1 and ethyl acetate. The layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined organic layers were washed two times with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, cyclohexane/AcOEt) to give 100 mg (0.24 mmol, 70%) of the title compound as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06969725B2
出典データセットuspto-grants-2005_11
ORD IDord-3dbcf44e59ee4ff99c88759e84e6073e
出典メモuspto-grants-2005_11