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HRID 860683作成日:2026年10月27日

1,2-Dichloroethane → (3-{1-Methyl-1-[4-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-ethylsulfanyl}-phenyl)-acetic Acid Methyl Ester

https://huagongshe.com/reaction/860683

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物Methyl 2-(3-mercaptophenyl)acetateHCID 14820216—
反応物2-[4-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-propan-2-olHCID 69589309—
触媒HCID 178506616HCID 178506616—
溶媒Ethyl AcetateHCID 8857—
生成物(3-{1-Methyl-1-[4-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-ethylsulfanyl}-phenyl)-acetic Acid Methyl EsterHCID 69589602—

反応手順

A mixture of 2-[4-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-propan-2-ol (0.1 g, 0.351 mmol), (3-Mercapto-phenyl)-acetic acid methyl ester (0.070 g, 0.386 mmol), zinc (I) iodide (0.056 g, 0.176 mmol), and 1,2-dichloroethane (2 mL) is stirred at room temperature 24 hr. The reaction mixture is diluted with ethyl acetate (25 mL), and washed with aqueous saturated sodium hydrogen carbonate, water, brine (25 mL each), dried over anhydrous magnesium sulfate, filtered, concentrated, and purified via silica chromatography eluting with 8:2 hexanes:ethyl acetate to afford the product as a colorless film, 0.105 g, 66%. MS M++1 286. The structure is confirmed by 1H NMR spectroscopy.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07153878B2
出典データセットuspto-grants-2006_12
ORD IDord-bab5aa22367e45bea9b2e2480dc93bae
出典メモuspto-grants-2006_12