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HRID 373003作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,4-Dichloro-1,3,5-triazineHCID 17810—
反応物Cesium fluorideHCID 25953—
反応物18-Crown-6HCID 28557—
反応物Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoateHCID 14326252—
溶媒Diethyl EtherHCID 3283—
溶媒AcetonitrileHCID 6342—
生成物(E)-methyl 2-[2-(4-chloro-1,3,5-triazin-2-yloxy)phenyl]-3-methoxypropenoateHCID 8674593465.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05162319
出典データセットuspto-grants-1992_11
ORD IDord-67f6a959f2314a1c9fe7483dce389599
出典メモuspto-grants-1992_11