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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130315생성일: 2026년 10월 27일

2,3,4,5-Tetrafluorobenzoyl chloride → Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate

https://huagongshe.com/reaction/130315

반응식

참여 물질

역할이름HCID투입량
반응물2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
반응물Potassium ethyl malonateHCID 3446434—
반응물Magnesium ChlorideHCID 5360315—
용매AcetonitrileHCID 6342—
생성물Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—

반응 단계

Potassium ethyl malonate (3.66 g, 21.5 mmol), MgCl2 (2.44 g, 25.7 mmol) and TEA (2.05 g, 20.3 mmol) were mixed in acetonitrile (70 ml) at 10-15° C. for 2.5 hr. 2,3,4,5-tetrafluorobenzoyl chloride (2.00 g, 10.3 mmol) in acetonitrile (10 ml) was added at 0° C. over 15 min followed by a second addition of TEA (0.23 g, 2.3 mmol). After allowing to warm to RT, the mixture was stirred for 16 hr. After removal of volatiles in vacculo Toluene (30 ml) was added and removed in vacuo. Following the addition of toluene (60 ml), HCl 1.5 M (40 ml) was added cautiously, ensuring the temperature did not exceed 25° C. The organic fraction was washed with HCl 1.5 M (2×25 ml) and water (2×25 ml), dried over MgSO4 and reduced to a light orange oil in vacuo ([M+1]+265, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381720B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-474bceeecd274ea987153a50a8377102
출처 메모uspto-grants-2008_06