関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2,4-Dichloro-1,3,5-triazine | HCID 17810 | — |
| 反応物 | Cesium fluoride | HCID 25953 | — |
| 反応物 | 18-Crown-6 | HCID 28557 | — |
| 反応物 | Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate | HCID 14326252 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (E)-methyl 2-[2-(4-chloro-1,3,5-triazin-2-yloxy)phenyl]-3-methoxypropenoate | HCID 86745934 | 65.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05162319 |
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| 出典データセット | uspto-grants-1992_11 |
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| ORD ID | ord-67f6a959f2314a1c9fe7483dce389599 |
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| 出典メモ | uspto-grants-1992_11 |
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