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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1753생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1753

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, 20% ether in dichloromethane) (3.52 g, 72%). mp 112°-114° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726315
출처 데이터셋uspto-grants-1998_03
ORD IDord-d167806c04b646d4b1c49664d0f6f7f3
출처 메모uspto-grants-1998_03