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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8972생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-BromothiazoleHCID 76430—
반응물4-Formylphenylboronic AcidHCID 591073—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물4-(1,3-Thiazol-2-yl)benzaldehydeHCID 1053565515%

반응 단계

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)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091217B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7a2f34a04f1b42dcbdbae8ab9077148c
출처 메모uspto-grants-2006_08