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HRID 14118생성일: 2026년 10월 26일

Oxazole → 3-(Methoxycarbonyl)-5-(1,3-oxazol-2-yl)benzoic Acid

https://huagongshe.com/reaction/14118

반응식

참여 물질

역할이름HCID투입량
반응물OxazoleHCID 9255—
반응물3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 15840391—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
생성물3-(Methoxycarbonyl)-5-(1,3-oxazol-2-yl)benzoic AcidHCID 21085836—

반응 조건

온도0 °C

반응 단계

To a −70° C. stirred solution of oxazole (432 mg, 6.3 mmol) in tetrahydrofuran (10 mL) is added n-butyllithium (2.5 M in hexanes, 2.75 mL, 6.9 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 18.75 mL, 18.75 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of 3-iodo-5-(methoxycarbonyl)benzoic acid prepared by the method in Example SP-281, step 1 (1.8 g, 6 mmol) in anhydrous tetrahydrofuran (10 mL) followed by palladium(0)tetrakis(triphenylphosphine) (291 mg, 0.25 mmol). The reaction mixture is heated at reflux for 15 h. The reaction mixture is cooled, filtered through diatomaceous earth, diluted with ethyl acetate (50 mL), washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 5% methanol/methylene chloride) provides the title compound in pure form. ESI MS m/z 246.1 [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5300a9569b4c4d14bd3a9b5cc261602e
출처 메모uspto-grants-2010_06