Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732877생성일: 2026년 10월 24일
N,N,N',N'-Tetramethylethylenediamine → 2-(Dicyclohexylphosphanyl)-1-(2,4,6-trimethylphenyl)-1H-imidazole
https://huagongshe.com/ko/reaction/732877
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | Chlorodicyclohexylphosphine | HCID 2734135 | — |
| 반응물 | 1-Mesityl-1h-imidazole | HCID 9815460 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 2-(Dicyclohexylphosphanyl)-1-(2,4,6-trimethylphenyl)-1H-imidazole | HCID 53411819 | — |
반응 단계
1.6 ml of TMEDA (15 mmol.) are added to a suspension of 1.86 g (10 mmol.) of N-mesitylimidazole in 30 ml of hexane. 6.25 ml of 1.6 molar n-butyllithium solution (10 mmol.) are added at room temperature. The mixture is then heated for 2.5 hours at reflux temperature (solution 1). In another flask, 2.2 ml (10 mmol.) of dicyclohexylchlorophosphane are mixed with 20 ml of hexane and heated to 60° C. (solution 2). The boiling solution 1 is then slowly transferred into solution 2, which is at 60° C., by means of a cannula. The mixture is then boiled for a further 1 hour at reflux, the solution is cooled, and 20 ml of degassed water are added thereto. The organic phase is filtered off over magnesium sulfate. The solution is concentrated in vacua; 30 ml of pentane are added thereto, and the mixture is boiled for 1 hour at reflux. The product precipitates in crystalline form at −30° C. and is filtered off while cold. Yield: 2.48 g (65%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07589081B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-4e99e6c803a0495f911d811494d36ce0 |
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| 출처 메모 | uspto-grants-2009_09 |
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