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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1690273생성일: 2026년 10월 27일

Tricyclohexylphosphine → Methyl 2-cyclopropyl-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/1690273

반응식

참여 물질

역할이름HCID투입량
반응물TricyclohexylphosphineHCID 75806—
반응물Cyclopropylboronic acidHCID 2760897—
반응물Potassium phosphate, tribasic, monohydrateHCID 22031701—
반응물Methyl 2-bromo-4-(trifluoromethyl)benzoateHCID 46311084—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물Methyl 2-cyclopropyl-4-(trifluoromethyl)benzoateHCID 5943848771%

반응 조건

온도100 °C

반응 단계

To a solution of 400 mg (1.413 mmol) 2-bromo-4-trifluoromethyl-benzoic acid methyl ester, 146 mg (1.696 mmol) cyclopropyl boronic acid, 1.21 g (4.946 mmol) tri-potassium phosphate monohydrate, 40.9 mg (0.141 mmol) tricyclohexyl phosphine in 6 ml toluene and 0.3 ml water under nitrogen at room temperature, was added 15.9 mg (0.0707 mmol) palladium acetate. The mixture was stirred in a 100° C. oil bath for 4 hours and overnight at room temperature under nitrogen. The mixture was cooled to room temperature. Water was added and the mixture extracted with ethyl acetate. The organic layer was washed once with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 10%) to provide 0.24 g (71%) of the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153653B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-0a806f7f6e524a92b72dc9a442dae54d
출처 메모uspto-grants-2012_04