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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 544189생성일: 2026년 10월 27일

Ethyl Bromide → 2-[[2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dione

https://huagongshe.com/reaction/544189

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물1,3-CyclopentanedioneHCID 77466—
반응물MagnesiumHCID 5462224—
반응물2-{4-[4-(Trifluoromethyl)phenoxy]phenoxy}propanoyl chlorideHCID 12906015—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-[[2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dioneHCID 13309168—

반응 단계

Ethyl bromide (6 g, 55 mmol) is added to magnesium turnings (1.34 g) in the presence of tetrahydrofuran (THF; 15 ml). After reaction is complete, the solution is diluted to 50 ml with THF cooled in an ice bath and cyclopentane-1,3-dione (50 mmol) is added rapidly with stirring. THF (250 ml) is added to this mixture and it is allowed to warm to RT. 2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionic acid chloride (55 mmol) is added dropwise with stirring, and the mixture is allowed to stand at RT for 30 minutes. It is then poured into a mixture of ice, water and ether. The aqueous layer is extracted several times with ether. The combined ether extracts are washed with water, dried over sodium sulfate and the solvent is removed to give 2-[[2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dione (V; Y is H, Z is CF3, R1 is CH3 and n is one). ##STR5##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04448965
출처 데이터셋uspto-grants-1984_05
ORD IDord-1139decdbd2847ce89daa9fbccd70d57
출처 메모uspto-grants-1984_05