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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | Diethyl chlorophosphate | HCID 13139 | — |
| 반응물 | 1,3-Dimethyl-2-(2-thienyl)imidazolidine | HCID 2797481 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [5-(1,3-Dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl ester | HCID 86659557 | 88.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08940927B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-56414b2da4aa423e8b2382c3272918d7 |
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| 출처 메모 | uspto-grants-2015_01 |
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