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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915781생성일: 2026년 10월 27일

Benzeneacetyl chloride, 4-bromo- → 1-Benzofuran-2-yl-2-(4-bromo-phenyl)-ethanone

https://huagongshe.com/reaction/915781

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneacetyl chloride, 4-bromo-HCID 181552—
반응물2-(Trimethylsilyl)benzofuranHCID 13148489—
촉매Titanium TetrachlorideHCID 24193—
용매DichloromethaneHCID 6344—
생성물1-Benzofuran-2-yl-2-(4-bromo-phenyl)-ethanoneHCID 5744111717.4%

반응 조건

온도-78 °C

반응 단계

Benzofuran-2-yl-trimethyl-silane (3.4 g, 17.86 mmol) was dissolved in methylene chloride (40 mL) and cool to −78° C. 4-Bromophenyl-acetyl chloride (19.65 mmol, 1.1 equiv.) was added at this temperature. Under vigorous stirring, a solution of TiCl4 (23 mL, 1M, 23.2 mmol, 1.3 equiv.) in CH2Cl2 was added dropwise and stirring continued for 20 min. Then the reaction was quenched with H2O (100 mL), cooling bath was removed and the mixture was allowed to warm up to room temperature. It was then diluted with H2O (100 mL) and extracted with CH2Cl2 (3×). Organic layers were combined, washed with brine, dried over MgSO4, solvent evaporated. Crude product thus obtained was subject to column purification. (silica gel, 10% EtOAC/Hexane). 980 mg of 1-Benzofuran-2-yl-2-(4-bromo-phenyl)-ethanone was obtained in 17% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07268135B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-cee734425971457484f01b14cf5b83bc
출처 메모uspto-grants-2007_09