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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270249생성일: 2026년 10월 24일

3-Fluoroanisole → (2-Fluoro-4-methoxy-phenyl)-(4-trifluoromethyl-phenyl)-methanone

https://huagongshe.com/ko/reaction/270249

반응식

참여 물질

역할이름HCID투입량
반응물3-FluoroanisoleHCID 9975—
반응물2-Fluoro-4-(trifluoromethyl)benzoyl chlorideHCID 145580—
반응물Aluminum(III) ChlorideHCID 6451240—
용매NitrobenzeneHCID 7416—
생성물(2-Fluoro-4-methoxy-phenyl)-(4-trifluoromethyl-phenyl)-methanoneHCID 2231403724%

반응 단계

1.4 l of nitrobenzene were cooled in an ice bath and treated in succession at a maximum temperature of 6° C. with 492.6 g (3.656 mol) of aluminum chloride and 700 g (3.355 mol) of 4-trifluoromethyl-2-fluoro-benzoyl chloride in 350 ml of nitrobenzene. The mixture was stirred (15 min) and 427.5 g (3.388 mol) of 3-fluoroanisole were added slowly so that the temperature did not rise above 6° C. The solution was left to warm to room temperature, stirred 2 h at this temperature, poured on to ice-water (2.5 l) and extracted with methylene chloride. The organic phase was washed with water and concentrated. After crystallization from THF (1.2l)/hexane (4.2l), 237 g (24%) of (2-Fluoro-4-methoxy-phenyl)-(4-trifluoromethyl-phenyl)-methanone were obtained, MS: 298 (M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449483B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-4027d4f3cd5445eda91a4d13f65a5c5d
출처 메모uspto-grants-2008_11