돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55258생성일: 2026년 10월 24일

Methyl Acrylate → (E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoate

https://huagongshe.com/ko/reaction/55258

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물Potassium CarbonateHCID 11430—
반응물3-Benzyloxy-2-iodopyridineHCID 19957501—
촉매Tetrabutylammonium BromideHCID 74236—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoateHCID 22161738—

반응 조건

온도100 °C

반응 단계

5.2 g of palladium(II) acetate, 77.8 g of potassium carbonate and 72.5 g of tetrabutylammonium bromide are added to a solution of 70 g of 3-benzyloxy-2-iodopyridine and 39.8 ml of acrylic acid methyl ester in 120 ml of dimethylformamide, and the suspension is stirred under argon atmosphere for 10 hours at 100° C. (bath temperature). The reaction mixture is concentrated by evaporation in a vacuum, the residue is added to water and shaken out with ethyl acetate. The organic phase is washed three times with water and once with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation. The crude product is chromatographed on silica gel with hexane/10-25% ethyl acetate. 48.2 g of 3-(3-benzyloxy-2-pyridyl)-(2E)-2-propenoic acid methyl ester is obtained as oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624943
출처 데이터셋uspto-grants-1997_04
ORD IDord-d4846378d04a4d3fb9385b65082d0c14
출처 메모uspto-grants-1997_04