関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethylene Glycol | HCID 174 | — |
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 4-Ethyl 1-methyl 3-oxopiperidine-1,4-dicarboxylate | HCID 10561371 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ethyl 1-methoxycarbonyl-3-oxopiperidine-4-carboxylate ethylene acetal | HCID 70082215 | — |
反応手順
A mixture of ethyl 1-methoxycarbonyl-3-oxopiperidine-4-carboxylate (9.0 g; 39 mmol), ethylene glycol (100 ml), 4-toluenesulfonic acid (0.7 g), and benzene (500 ml) was refluxed for 6 days using a Dean-Stark water separator. The mixture was washed with aqueous sodium carbonate (300 ml; 1 M), water (300 ml), and saturated aqueous sodium chloride (300 ml). The organic phase was dried (K2CO3) and evaporated in vacuo to give 8.6 of an oil. CC [silica gel (Woelm 0.063-0.1 mm): 350 g; eluents: methylene chloride to which ethyl acetate (20-35%) was added] followed by ball-tube distillation at 40 Pa (oven temperature 170° C.) gave VIIIa (7.0 g; 65%) as a colourless oil. IR (film): 2970 (s), 2900 (s), 1730 (s) cm-1. 1H NMR (CCl4): δ4.05 (q, J 7 Hz) and 3.92 (s) (a total of 6H), 3.60 (s) and 3.7-3.0 (m) (a total of 7H), 2.8-2.5 (1H, t), 2.2-1.6 (2H, m), 1.23 (3H, t, J 7 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04278676 |
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| 出典データセット | uspto-grants-1981_07 |
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| ORD ID | ord-c770ce4d92344889aecaa4794dfd3ee7 |
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| 出典メモ | uspto-grants-1981_07 |
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