戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 43136作成日:2026年10月23日

Ethylenediamine → 2-Piperazinone, 3,3-dimethyl-

https://huagongshe.com/ja/reaction/43136

反応式

関与物質

役割名称HCID仕込み量
反応物EthylenediamineHCID 3301—
反応物Potassium CarbonateHCID 11430—
反応物Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
溶媒TolueneHCID 1140—
生成物2-Piperazinone, 3,3-dimethyl-HCID 21115765.6%

反応手順

A mixture of ethyl-2-bromoisobutyrate (14.6 g, 74.9 mmol), ethylene diamine (33 mL, 487 mmol, 6.5 equiv) and potassium carbonate (11.4 g, 82.4 mmol, 1.1 equiv) in toluene (150 mL) was stirred for 22 h at reflux, cooled and filtered. The filtrate was concentrated and the residue triturated in Et2O to afford 6.3 g of 3,3-dimethyl-piperazin-2-one as a white solid. Methyl iodide (4 mL, 64.0 mmol, 1.3 equiv) was added dropwise to a suspension of 3,3-dimethyl-piperazin-2-one (6.3 g, 49.2 mmol) and potassium carbonate (8.8 g, 64.0 mmol, 1.3 equiv) in DME (20 mL). The reaction mixture was heated to 45° C., stirred for 3 h, cooled and filtered, washing the filter cake with DME. The filtrate was concentrated and the residue triturated in DME to afford 2.8 g (batch 1) of the title compound as a white solid. The filtrate from the trituration was concentrated and the residue purified by silica gel column chromatography (DCM/MeOH, 9:1) to afford 1.75 g (batch 2) of the title compound as a white solid. Title compound: ESI-MS: 143.1 [M+H]+; TLC: Rf=0.25 (DCM/MeOH, 9:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536175B2
出典データセットuspto-grants-2013_09
ORD IDord-e901742aa3bc4db58580aec9d1ab2a9d
出典メモuspto-grants-2013_09