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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9344생성일: 2026년 10월 23일

Triphenylphosphine → {4-[3,3-Bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester

https://huagongshe.com/ko/reaction/9344

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물3,3-Bis-(4-pyridin-3-yl-phenyl)-prop-2-en-1-olHCID 21986819—
반응물Ethyl [4-sulfanyl-2-(trifluoromethyl)phenoxy]acetateHCID 59516001—
용매TetrahydrofuranHCID 8028—
생성물{4-[3,3-Bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl esterHCID 69620630—

반응 단계

Triphenylphosphine (138 mg, 0.68 mmol) and ADDP (173 mg, 0.68 mmol) were added to a solution of 3,3-bis-(4-pyridin-3-yl-phenyl)-prop-2-en-1-ol (100 mg, 0.27 mmol) in THF (5 ml) at 0° C. The reaction mixture was stirred for 5 min under nitrogen atmosphere. (4-Mercapto-2-trifluoromethyl-phenoxy)-acetic acid ethyl ester (prepared analogous to procedure in BioOrg. Med. Chem. Lett. 2003, 13, 1517) (92 mg, 0.32 mmol) was slowly added to the reaction mixture and the reaction was stirred for further 2 h at 0° C. The reaction mixture was evaporated and the residue was triturated with ether (2×15 ml). The filtered ether phases were evaporated and purified by column chromatography (eluent: ethyl acetate) to give {4-[3,3-bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester in 100 mg (60%) yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091245B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c5ebe0b0aed846cc89d4466e7663f9a1
출처 메모uspto-grants-2006_08