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HRID 1431004作成日:2026年10月27日

N,N,N',N'-Tetramethylethylenediamine → [5-(1,3-Dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl ester

https://huagongshe.com/reaction/1431004

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物Diethyl chlorophosphateHCID 13139—
反応物1,3-Dimethyl-2-(2-thienyl)imidazolidineHCID 2797481—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物[5-(1,3-Dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl esterHCID 8665955788.7%

反応条件

温度-78 °C

反応手順

To a solution of 1,3-Dimethyl-2-thiophen-2-yl-imidazolidine (10 g, 60.17 mmol) in THF was added TMEDA (9.1 ml, 60.17 mmol), cooled to −78° C., then added 1.6 M nBuLi (47 ml, 75.21 mmol). After stirring at −78° C. for 30 min the mixture was warmed up to 0° C. in 1 hr and treated with diethyl chlorophosphonate (10.4 ml, 72.2 mmol). The reaction mixture was stirred at 0° C. for another 30 min. The reaction was then quenched by adding EtOAc and water. The EtOAc layer was separated and the water layer was further extracted with EOAc once. The combined EtOAc layers were dried over MgSO4, filtrated and concentrated to afford the crude product [5-(1,3-dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl ester (17 g). 1H NMR (300 MHz, DMSO-d6): δ 7.44 (m, 1H), 7.24 (m, 1H). 4.01 (m, 4H), 3.18 (m, 2H), 2.53 (m, 2H), 1.22 (m, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08940927B2
出典データセットuspto-grants-2015_01
ORD IDord-56414b2da4aa423e8b2382c3272918d7
出典メモuspto-grants-2015_01