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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500133생성일: 2026년 10월 26일

N,N,N',N'-Tetramethylethylenediamine → 4-Acetyl-2-fluorobenzonitrile

https://huagongshe.com/reaction/500133

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물1-(4-Bromo-3-fluorophenyl)ethan-1-oneHCID 22831914—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylformamideHCID 6228—
생성물4-Acetyl-2-fluorobenzonitrileHCID 22481653—

반응 조건

온도160 °C

반응 단계

N,N,N′,N′-Tetramethylethylenediamine (0.667 mL, 4.42 mmol), zinc cyanide (1.46 g, 12.4 mmol), tris(dibenzylideneacetone)dipalladium(0) (54.05 mg, 0.059 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (124.3 mg, 0.215 mmol) was added successively to a solution of 1-(4-bromo-3-fluorophenyl)ethanone (4.34 g, 20.0 mmol) in N,N-dimethylformamide (15 mL) in a microwave tube. The tube was sealed and degassed three times, and heated to 160° C. under microwave irradiation with a 240 s hold time, and 300 Watt maximum power input. After cooling, the reaction mixture was filtered through a pad of Celite with a thin layer of silica gel in the middle using dichloromethane as the eluant. The combined filtrates were concentrated under reduced pressure. The residue was purified by chromatography on silica gel with ethyl acetate in hexanes (0-40%) to give the desired product. (3.20 g, 98.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767675B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-77ff4e5b5c7244ae8e31d1c30552ca0c
출처 메모uspto-grants-2010_08