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HRID 14118作成日:2026年10月26日

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

https://huagongshe.com/reaction/14118

反応式

関与物質

役割名称HCID仕込み量
反応物OxazoleHCID 9255—
反応物3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 15840391—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
生成物3-(Methoxycarbonyl)-5-(1,3-oxazol-2-yl)benzoic AcidHCID 21085836—

反応条件

温度0 °C

反応手順

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]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-5300a9569b4c4d14bd3a9b5cc261602e
出典メモuspto-grants-2010_06