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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128484생성일: 2026년 10월 24일

Potassium Carbonate → Acifluorfen-methyl

https://huagongshe.com/ko/reaction/128484

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
반응물5-Fluoro-2-nitrobenzoic acid methyl esterHCID 5152049—
용매Dimethyl SulfoxideHCID 679—
생성물Acifluorfen-methylHCID 9164284%

반응 단계

To a 5-liter, 4-necked flask fitted with a stirrer, thermometer, addition funnel, reflux condenser and drying tube is added dimethyl sulfoxide (200 ml), 2-chloro-4-trifluoromethylphenol) (715 g, 3.64 mole), and anhydrous potassium carbonate (520 g, 3.72 moles). The reaction mixture is stirred at room temperature overnight under a nitrogen atmosphere. Then methyl 5-fluoro-2-nitrobenzoate (724 g, 3.64 moles) is added over a 1 hour period (slight exotherm to 31° C.). After stirring overnight at room temperature, the inorganic solids are removed by filtration and 1700 ml of dimethyl sulfoxide removed under vacuum (1 mm, pot temp. of 85° C., vapor temp. of -40° C.). The residue is diluted with a large volume of carbon tetrachloride and water washed. The organic layer is dried with anhydrous magnesium sulfate and the solvent removed under vacuum to afford 1142 g of methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate (84% yield). Anal. Calcd. for C15H9ClF3NO5 : C, 47.90; H, 2.42; Cl, 9.45; F, 15.20; N, 3.73. Found: C, 47.83; H, 2.47; Cl, 9.15; L F, 14.84; N, 3.69.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04259510
출처 데이터셋uspto-grants-1981_03
ORD IDord-7d47697a8a054a53b36c6a9edd237aff
출처 메모uspto-grants-1981_03