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HRID 399807作成日:2026年10月26日

Methyl 3-iodobenzoate → Methyl 3-[2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)phenyl]benzoate

https://huagongshe.com/reaction/399807

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-iodobenzoateHCID 69258—
反応物Potassium FluorideHCID 522689—
反応物1-Tri(n-butyl)stannyl-2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)benzeneHCID 18945295—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 3-[2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)phenyl]benzoateHCID 1894530514.4%

反応手順

A suspension of 1-tri(n-butyl)stannyl-2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)benzene (5 g), methyl 3-iodobenzoate (2.17 g) and tetrakis(triphenylphosphine) palladium(0) (0.29 g) in dioxane was refluxed for 18 hours. After being cooled to room temperature, 25% potassium fluoride aqueous solution (11 ml) was added to the reaction mixture and the mixture was stirred for 15 minutes. Insoluble material was filtered by using celite The filtrate was extracted with ethyl acetate (50 ml), washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuo. The residue was purified by column chromatography on silica gel (200 g) with benzene-ethyl acetate (20:1) as an eluent. The fractions containing the object compound were combined and evaporated in vacuo. The residue was recrystallized from methanol to afford methyl 3-[2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)phenyl]benzoate (370 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05824691
出典データセットuspto-grants-1998_10
ORD IDord-43898460293b4aadbbd077910ed57161
出典メモuspto-grants-1998_10