돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1431004생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1431004

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물Diethyl chlorophosphateHCID 13139—
반응물1,3-Dimethyl-2-(2-thienyl)imidazolidineHCID 2797481—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물[5-(1,3-Dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl esterHCID 8665955788.7%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08940927B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-56414b2da4aa423e8b2382c3272918d7
출처 메모uspto-grants-2015_01