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HRID 8972作成日:2026年10月23日

Potassium Carbonate → 4-(1,3-Thiazol-2-yl)benzaldehyde

https://huagongshe.com/ja/reaction/8972

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-BromothiazoleHCID 76430—
反応物4-Formylphenylboronic AcidHCID 591073—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物4-(1,3-Thiazol-2-yl)benzaldehydeHCID 1053565515%

反応手順

To a solution of 2-bromothiazole (0.26 g, 1.6 mmol) and 4-formylphenylboronic acid (0.48 g, 3.2 mmol) in toluene (16 mL) was added tetrakis(triphenylphosphine)palladium(0) (0.09 g, 0.08 mmol) and K2CO3 (0.33 g, 2.4 mmol) and the solution stirred at reflux for 16 h. The reaction was cooled to room temperature, diluted with water (50 mL) and ethyl acetate (50 mL). The organic layer was separated, washed with brine (30 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (2% MeOH/CH2Cl2) to give 4-(2-thiazolyl)-benzaldehyde (45 mg, 15%). 1H NMR (CDCl3) δ 7.45 (d, 1H, J=3.0 Hz), 7.90 (d, 1H, J=3.0 Hz), 7.97 (d, 2H, J=7.8 Hz), 8.15 (d, 2H, J=7.2 Hz), 10.07 (s, 1H (CHO)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091217B2
出典データセットuspto-grants-2006_08
ORD IDord-7a2f34a04f1b42dcbdbae8ab9077148c
出典メモuspto-grants-2006_08