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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373003생성일: 2026년 10월 24일

Potassium Carbonate → (E)-methyl 2-[2-(4-chloro-1,3,5-triazin-2-yloxy)phenyl]-3-methoxypropenoate

https://huagongshe.com/ko/reaction/373003

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,4-Dichloro-1,3,5-triazineHCID 17810—
반응물Cesium fluorideHCID 25953—
반응물18-Crown-6HCID 28557—
반응물Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoateHCID 14326252—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물(E)-methyl 2-[2-(4-chloro-1,3,5-triazin-2-yloxy)phenyl]-3-methoxypropenoateHCID 8674593465.3%

반응 단계

To a stirred solution of 2,6-dichloro-1,3,5-triazine (0.3 g, 2 mmol; made according to R L N Harris, Synthesis, 1981, 907) and potassium carbonate (0.28 g, 2 mmol) in dry acetonitrile (25 ml) at 0° C. under an atmosphere of nitrogen was added dropwise a solution of (E)-methyl 2-(2-hydroxyphenyl)-3-methoxypropenoate (0.42 g, 2 mmol) in dry acetonitrile (7 ml). Anhydrous caesium fluoride (0.30 g, 2 mmol) and a catalytic amount of 18-crown-6 were added with stirring and the temperature was allowed to rise to room temperature. After stirring overnight, the reaction mixture was filtered and evaporated to leave a yellow/orange paste. Chromatography (eluent diethyl ether) afforded (E)-methyl 2-[2-(4-chloro-1,3,5-triazin-2-yloxy)phenyl]-3-methoxypropenoate (0.42 g) as a white solid, m.p. 137°-140° C.; Infrared max. 1704, 1631 cm-1 ; 1H NMR (CDCl3) δ 3.63(3 H,s); 3.75(3H,s); 7.19-7.29(1H,m); 7.31-7.45(3H,m); 7.47(1H,s); 8.74(1H,s) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162319
출처 데이터셋uspto-grants-1992_11
ORD IDord-67f6a959f2314a1c9fe7483dce389599
출처 메모uspto-grants-1992_11