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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490776생성일: 2026년 10월 24일

Tributylphosphine → 3-{2-Methyl-4-[5-(4-trifluoromethyl-phenyl)-thiophen-2-ylmethoxy]-phenyl}-propionic acid methyl ester

https://huagongshe.com/ko/reaction/490776

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Methyl 3-(4-Hydroxy-2-methylphenyl)propanoateHCID 13551833—
반응물2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-HCID 21986352—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
생성물3-{2-Methyl-4-[5-(4-trifluoromethyl-phenyl)-thiophen-2-ylmethoxy]-phenyl}-propionic acid methyl esterHCID 68853010—

반응 단계

To a solution of [5-(4-Trifluoromethyl-phenyl)-thiophen-2-yl]-methanol (0.063 g, 0.232 mmole) and 3-(4-Hydroxy-2-methyl-phenyl)-propionic acid methyl ester (0.045 g, 0.232 mmole) in toluene (2 mL) at room temperature, is added tributylphosphine (0.087 mL, 0.348 mmole) followed by a solution of 1,1′-(azodicarbonyl)-dipiperidine (0.088 g, 0.348 mmole) in toluene (2 mL). The reaction is stirred overnight, and then diluted with hexane (10 mL). The precipitate is removed through filtration and the filtrate is concentrated, loaded to a silica gel column, eluted with ethyl acetate in hexane (0-15%) and concentrated to provide the titled compound as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528160B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-214e20cfb29941c9930ae7b36710846b
출처 메모uspto-grants-2009_05