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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325594생성일: 2026년 10월 27일

1-Chloro-4-(trifluoromethyl)benzene → 2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate

https://huagongshe.com/reaction/325594

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
반응물Potassium CarbonateHCID 11430—
반응물2-(2-Fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionateHCID 13278922—
용매DimethylformamideHCID 6228—
생성물2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionateHCID 13132188—

반응 조건

온도95 °C

반응 단계

33.4 g of 2-(2-fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionate was dissolved in 120 ml of dimethylformamide, 15.2 g of potassium carbonate were added thereto, then the mixture was heated at 95° C. for one hour with stirring. 27.1 g of 4-trifluoromethyl chlorobenzene were added to the solution which was then heated to 95° to 100° C. for five hours. After cooling the reaction solution to room temperature, it was poured into ice-water, then extracted with toluene. The toluene layer was washed successively with 1% strength by weight sodium hydroxide solution and water, and was dried and filtered. The toluene was distilled off under reduced pressure, and further volatile by-products were removed at 100° C./0.1 mmHg. The end product of 2-(2-fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate was obtained in a yield of 20.7 g. (nD20 1.5235)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04441913
출처 데이터셋uspto-grants-1984_04
ORD IDord-917c4f4b5fc74a62becab5a37151707f
출처 메모uspto-grants-1984_04