戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 348889作成日:2026年10月27日

Thiazole → Methyl 4-(thiazol-2-Yl)benzoate

https://huagongshe.com/reaction/348889

反応式

関与物質

役割名称HCID仕込み量
反応物ThiazoleHCID 9256—
反応物Methyl 4-iodobenzoateHCID 69273—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(thiazol-2-Yl)benzoateHCID 11241445—

反応条件

温度0 °C

反応手順

To a −70° C., stirred solution of thiazole (270 μL, 3.8 mmol) in tetrahydrofuran (10 mL) is added n-butyl lithium (2.6 mL of a 1.6 M solution in hexanes, 4.2 mmol). After 30 min, zinc chloride (11.4 mL of a 1.0 M solution in diethyl ether, 11.4 mmol) is added. The reaction mixture is warmed to 0° C. and methyl 4-iodobenzoate (1 g, 3.8 mmol) and palladium(0) tetrakis(triphenylphosphine) (530 mg, 0.4 mmol) are added. The reaction mixture is heated at 70° C. for 20 h under argon, cooled to room temperature, and then partitioned between ethyl acetate and water. The organic layer is washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (3:1 hexanes/ethyl acetate) yields the title compound. 1H NMR (300 MHz, CDCl3) δ 8.14–8.03 (m, 4H), 7.93–7.92 (m, 1H), 7.42–7.41 (m, 1H), 3.95 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176242B2
出典データセットuspto-grants-2007_02
ORD IDord-2bac21ef6e944361a45ad2faa71ba177
出典メモuspto-grants-2007_02