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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513128생성일: 2026년 10월 26일

Formic Acid → [3-[4-Chloro-2-(2-fluorobenzoyl)-phenyl]-3-oxopropyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/513128

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참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물{3-[4-Chloro-2-(2-fluoro-benzoyl)-phenyl]-prop-2-ynyl}-carbamic acid tert-butyl esterHCID 67505268—
촉매Mercuric sulfateHCID 24544—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ammonium HydroxideHCID 14923—
생성물[3-[4-Chloro-2-(2-fluorobenzoyl)-phenyl]-3-oxopropyl]-carbamic acid tert-butyl esterHCID 6750545995%

반응 조건

온도0 °C

반응 단계

A solution of {3-[4-chloro-2-(2-fluoro-benzoyl)-phenyl]-prop-2-ynyl}-carbamic acid tert-butyl ester (9.2 g, 23 mmol) in CH2Cl2 (100 mL) containing formic acid (9.18 mL) was cooled to 0° C. Mercury(II) sulphate (2.1 g, 7.1 mmol) was added and the reaction stirred for 2 h at 0° C. The mixture was diluted with H2O (20 mL) and NH4OH (20 mL). The organic phase was collected and the aqueous phase was extracted with EtOAc (3×100 mL). The combined organic portions were washed with H2O, dried over MgSO4, filtered and the solvents evaporated in vacuo to afford [3-[4-chloro-2-(2-fluorobenzoyl)-phenyl]-3-oxopropyl]-carbamic acid tert-butyl ester 8.9 g (95%) as a brown solid. This material (8.9 g, 22 mmol) was dissolved in HCl (4N in dioxane, 185 mL) and stirred at room temperature for 30 min. The solution was then evaporated in vacuo. The residue was dissolved in CH2Cl2 (250 mL) and diisopropylethylamine amine (18 mL) was added. The solution was stirred at room temperature for 2 h. The solution was evaporated in vacuo and the residue purified by column chromatography (silica gel, 10 to 50% EtOAc/hexanes) to provide 4k (2.9 g, 46%) as a brown solid MS m/z=288 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102678B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-ccd446c6f6fe4c64b373899017c3cb5e
출처 메모uspto-grants-2015_08