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HRID 1277630作成日:2026年10月27日

Ethylene Glycol → Ethyl 1-methoxycarbonyl-3-oxopiperidine-4-carboxylate ethylene acetal

https://huagongshe.com/reaction/1277630

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物BenzeneHCID 241—
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-Ethyl 1-methyl 3-oxopiperidine-1,4-dicarboxylateHCID 10561371—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 1-methoxycarbonyl-3-oxopiperidine-4-carboxylate ethylene acetalHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04278676
出典データセットuspto-grants-1981_07
ORD IDord-c770ce4d92344889aecaa4794dfd3ee7
出典メモuspto-grants-1981_07