関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Diethyl 2-(ethoxymethylidene)-3-oxobutanedioate | HCID 40590 | — |
| 反応物 | 1-Morpholinobutene | HCID 580977 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Diethyl 5-ethylpyridine-2,3-dicarboxylate | HCID 10857926 | — |
反応手順
To a solution of diethyl ethoxymethyleneoxalacetate (43.2 g, 0.16 mol) dissolved in CH3OH (150 mL) at -10° under N2 is added 1-morpholinobutene (25 g, 0.16 mol). The reaction is slowly warmed to room temperature over three hours, after which the CH3OH is removed in vacuo. The residue is dissolved in acetic acid (100 mL) and this solution slowly added to NH4Cl (34.2 g, 0.64 mol) dissolved in acetic acid (200 mL) at 50°-70°. The reaction is then heated to 90°-95° for two hours and 30 minutes, concentrated in vacuo, partitioned between water and the CH2Cl2, and the organic phase chromatographed over silica gel with CH2Cl2 -CH3CN (95:5) elution to give the product as an oil. Distillation at 123°-155° at 0.15mm gives the product (23.4 g, 83% pure, 55%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05565411 |
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| 出典データセット | uspto-grants-1996_10 |
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| ORD ID | ord-357bccaf74ba402e87f805796aa3aa07 |
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| 出典メモ | uspto-grants-1996_10 |
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