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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490770생성일: 2026년 10월 25일

Tributylphosphine → (6-{2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-ethoxy}-benzofuran-3-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/490770

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Methyl 2-(6-hydroxy-1-benzofuran-3-yl)acetateHCID 20770861—
반응물2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-ethanolHCID 22647490—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물(6-{2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-ethoxy}-benzofuran-3-yl)-acetic acid methyl esterHCID 5767548233%

반응 단계

To a solution of 2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-ethanol (0.12 g, 0.43 mmol) in toluene (3 mL) at 0° C. is added ADDP (0.14 g, 0.57 mmol) followed by tri-n-butylphosphine (0.14 mL, 0.56 mmol). A toluene solution of (6-Hydroxy-benzofuran-3-yl)-acetic acid methyl ester (0.52 g, 1.22 mmol) is added, and the mixture is allowed to warm to RT overnight. Water is added, and the aqueous phase is extracted with EtOAc. The organics are dried with MgSO4 and purified by flash chromatography to yield the title compound (0.066 g, 33%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528160B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-1e39dc89aa9343e1bbf5e362de2afa7f
출처 메모uspto-grants-2009_05