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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23519생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanone

https://huagongshe.com/ko/reaction/23519

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Benzoic acid, 4-fluoro-, ethyl esterHCID 67976—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물2-Fluoro-4-methylpyridineHCID 2737403—
생성물1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanoneHCID 11031769—

반응 단계

To a solution of sodium bis(trimethylsilyl)amide (0.465 L, 1M) in TBF (765 mL) under nitrogen, cooled to 2° C., was added 2-fluoro-4-methylpyridine (25 g, 0.225 mol) and the solution stirred for 45 minutes in an ice bath. Ethyl 4-fluoro-benzoate (35 mL, 0.239 mol) was added and the reaction was stirred for 1.5 hours at RT. The reaction mixture was poured into excess aqueous 2N HCl, and the aqueous layer was made basic with 5 N NaOH and extracted with EtOAc. The organic extracts were combined, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and filtered through a cotton plug. Hexanes were added and the CH2Cl2 was removed under reduced pressure until precipitation of the title compound occurred as a pale yellow solid (43.2 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852727B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8b2ce258c09b4c8d8cddd43a27d5f774
출처 메모uspto-grants-2005_02