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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399807생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/399807

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-iodobenzoateHCID 69258—
반응물Potassium FluorideHCID 522689—
반응물1-Tri(n-butyl)stannyl-2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)benzeneHCID 18945295—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매1,4-DioxaneHCID 31275—
생성물Methyl 3-[2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)phenyl]benzoateHCID 1894530514.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05824691
출처 데이터셋uspto-grants-1998_10
ORD IDord-43898460293b4aadbbd077910ed57161
출처 메모uspto-grants-1998_10