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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 860701생성일: 2026년 10월 25일

Tributylphosphine → 3-(4-{1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethoxy}-2-methyl-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/860701

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Methyl 3-(4-Hydroxy-2-methylphenyl)propanoateHCID 13551833—
반응물1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanolHCID 58765664—
용매TolueneHCID 1140—
생성물3-(4-{1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethoxy}-2-methyl-phenyl)-propionic acid methyl esterHCID 1015213883.1%

반응 단계

A solution of 3-(4-hydroxy-2-methyl-phenyl)-propionic acid methyl ester (6.30 g, 32.1 mmol) and 1-[2-(4-bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanol (9.05 g, 29.2 mmol) in toluene (300 mL) is degassed and filled with nitrogen for 3 times. Tributylphosphine (7.70 g, 38.1 mmol) is added to the reaction mixture under nitrogen at 0° C., followed by addition of of 1,1′-(azodicarbonyl)-dipiperidine (8.84 g, 35.0 mmol). The reaction mixture is allowed to warm to room temperature and stirred overnight, the mixture is loaded directly on silica gel column chromatography with 10–15% EtOAc/Hexanes to afford the title compound (11.8 g, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07153878B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-3be89de06aa04407b92b958c9d1c264f
출처 메모uspto-grants-2006_12