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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 126970생성일: 2026년 10월 25일

Chlorobenzene → Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate

https://huagongshe.com/reaction/126970

반응식

참여 물질

역할이름HCID투입량
반응물ChlorobenzeneHCID 7964—
반응물Potassium CarbonateHCID 11430—
반응물p-(4-(Trifluoromethyl)phenoxy)phenolHCID 170230—
반응물Ethyl 4-bromopent-2-enoateHCID 53952747—
촉매N,N-Dibutyl-N-ethylbutan-1-aminium bromideHCID 19043781—
용매WaterHCID 962—
생성물Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoateHCID 15692196%

반응 단계

In a reactor, 100 ml of chlorobenzene and 100 ml of water were charged and then, 95.3 g (0.375 mole) of 4-(4-trifluoromethylphenoxy)phenol, 85.4 g (0.412 mole) of ethyl 4-bromo-2-pentenoate, 39.0 g (0.281 mole) of potassium carbonate and 1.1 g (0.00375 mole) of tributylethyl ammonium bromide were added. The mixture was refluxed with stirring for 6 hours to react them, and the water phase was removed and the organic phase was washed with 5% hydrochloric acid and with water and then, chlorobenzene, ethyl 4-bromo-2-pentenoate and low boiling by-products were distilled off at 100° C. under a reduced pressure of 0.02 to 0.05 mmHg to obtain 137.0 g of ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate. The yield was 96.0%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254262
출처 데이터셋uspto-grants-1981_03
ORD IDord-8cc3e1a347fb4f15b35b9cd8dfe0e993
출처 메모uspto-grants-1981_03