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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1458480생성일: 2026년 10월 27일

Thiophene → 4-(Thiophen-2-yl)benzaldehyde

https://huagongshe.com/reaction/1458480

반응식

참여 물질

역할이름HCID투입량
반응물ThiopheneHCID 8030—
반응물4-BromobenzaldehydeHCID 70741—
반응물Potassium AcetateHCID 517044—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매DimethylacetamideHCID 31374—
생성물4-(Thiophen-2-yl)benzaldehydeHCID 736499—

반응 조건

온도150 °C

반응 단계

3.7 g (20 mmol) of 4-bromobenzaldehyde, 9.5 ml (120 mmol) of thiophene, 2.94 g (30 mmol) of potassium acetate and 1.16 g (1 mmol) of tetrakis(triphenylphosphine)-palladium (Fluka, Buchs, Switzerland) in 50 ml of dimethylacetamide are placed in a pressure reactor and stirred at 150° C. under nitrogen for 16 hours. The reaction mixture is concentrated by evaporation; the residue is taken up in water and extracted three times with methylene chloride. After removal of the solvent, the residue is chromatographed on silica gel (hexane/ethyl acetate 4:1). The title compound is obtained in the form of a yellow solid. TLC: Rt 0.36 (hexane/ethyl acetate 4:1). HPLC20-100 : tRet =15.26. 1H-NMR (CD3OD; 200 MHz): 9.98/s (1H); 7.93 and 7.85/each d, J=9.5 (2×2H); 7.60/d, J=2.5 (1H); 7.52/d, J=5 (1H); 7.17/d×d, J=2.5 and 5 (1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05849911
출처 데이터셋uspto-grants-1998_12
ORD IDord-02410a55293242be982f4ecebcfbf643
출처 메모uspto-grants-1998_12