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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752생성일: 2026년 10월 23일

Diethyl Ether → t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate

https://huagongshe.com/ko/reaction/1752

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물tert-Butyl acrylateHCID 15458—
반응물Potassium AcetateHCID 517044—
반응물2-Bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridineHCID 19692711—
촉매Tetrabutylammonium IodideHCID 67553—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoateHCID 54231524—

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 (3.00 g, 30.6 mmol), tetra-n-butylammonium iodide (4.36 g, 11.8 mmol), bis(triphenylphosphine)palladium dichloride (0.33 g, 0.47 mmol) and t-butyl acrylate (6.16 g, 48 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 45 min. The mixture was cooled and added to water (250 ml). The product was extracted into ethyl acetate (2×60 ml). The combined extracts were washed with water (100 ml), 5% sodium chloride solution (2×100 ml), then dried and evaporated. The product was obtained by flash column chromatography using silica and 10% ether in dichloromethane. Yield 4.29 g, 77%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726315
출처 데이터셋uspto-grants-1998_03
ORD IDord-518c5ae80b704ac1999ffc9853c652ad
출처 메모uspto-grants-1998_03