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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

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물ChlorodicyclohexylphosphineHCID 2734135—
반응물1-Mesityl-1h-imidazoleHCID 9815460—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매HexaneHCID 8058—
생성물2-(Dicyclohexylphosphanyl)-1-(2,4,6-trimethylphenyl)-1H-imidazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589081B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-4e99e6c803a0495f911d811494d36ce0
출처 메모uspto-grants-2009_09