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HRID 338765作成日:2026年10月25日

Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride → Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate

https://huagongshe.com/reaction/338765

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 102623—
反応物Sodium BicarbonateHCID 516892—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 1-benzyl-4-oxopiperidine-3-carboxylateHCID 10262492%

反応手順

In a 5 L 3-necked flask equipped with a mechanical stirrer and a dropping funnel was placed ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate hydrochloride, (199.3 g, 0.67 mol) in dichloromethane (1.5 L). To this suspension was added saturated sodium bicarbonate (1.5 L) over one hour. After the solid dissolved, the organic layer was separated, washed with brine (250 mL), filtered through 1 PS filter paper and concentrated under reduced pressure to give 160.5 g (92%) of ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate as an oil. NMR 60 MHz, (CDCl3), δ 7.3 (s, 5H), 4.2 (q, 2H), 3.6 (s, 2H), 2.3-3.6 (m, 6H), 1.3 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889870B2
出典データセットuspto-grants-2014_11
ORD IDord-23accd3ce0b947b5adda01e15ea94ba1
出典メモuspto-grants-2014_11