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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264786생성일: 2026년 10월 26일

Triphenylphosphine → 3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic Acid

https://huagongshe.com/reaction/264786

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Potassium AcetateHCID 517044—
반응물Potassium acrylateHCID 4429391—
반응물2-Bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridineHCID 19692711—
촉매Palladium ChlorideHCID 24290—
촉매Tetrabutylammonium IodideHCID 67553—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic AcidHCID 54021897—

반응 조건

온도120 °C

반응 단계

To a solution of 2-bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridine (5.00 g, 11.8 mmol) in DMF (22.8 ml) and water (1.2 ml) were added potassium acetate (2.91 g, 29.7 mmol), tetra-n-butylammonium iodide (4.37 g, 11.8 mmol), triphenylphosphine (0,245 g, 0.94 mmol), palladium chloride (83 mg, 0.47 mmol) and potassium acrylate (3.91 g, 35.4 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 3.3 h. Some potassium acrylate remained undissolved. The mixture was cooled, solids filtered and washed with ethyl acetate (2×60 ml). The filtrate was washed with water (250 ml) and with 5% sodium chloride solution (2×125 ml). The organic layer was dried and evaporated. The pure product was obtained by flash column chromatography (silica, 2,0% ether in dichloromethane) (3.52 g, 72%). mp 112°114° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646286
출처 데이터셋uspto-grants-1997_07
ORD IDord-ea78dff7ba164da1b7519d695e39162b
출처 메모uspto-grants-1997_07