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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381819생성일: 2026년 10월 26일

4-Fluorobiphenyl → Methyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrate

https://huagongshe.com/reaction/381819

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobiphenylHCID 9461—
반응물Butanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrateHCID 1554112074.6%

반응 단계

To a stirred suspension of anhydrous aluminum chloride (9.64 g, 0.723 mol) in dichloromethane (90 mL) at 5° C. was added dropwise a solution of 4-fluorobiphenyl (4.97 g, 0.0289 mol) in dichloromethane (40 mL) followed by the dropwise addition of a solution of 3-carbomethoxypropionyl chloride (3.94 mL, 0.032 mol) in dichloromethane (30 mL), and the mixture stirred. After 2 hours at 5° C., the mixture was allowed to warm to room temperature. After 1 day, the reaction was cooled to 5° C. and quenched by the dropwise addition of water (160 mL). The layers were separated, and the organic layer washed with brine, dried (Na2SO4), and rotary evaporated. The residue was recrystallized from methanol (300 mL) to give 6.17 g of 4-(4′-fluoro-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a pale yellow solid; mp 131.5-133.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06307089B2
출처 데이터셋uspto-grants-2001_10
ORD IDord-e554754d25da4b91b1ad3a91d61b2761
출처 메모uspto-grants-2001_10