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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732876생성일: 2026년 10월 24일

N,N,N',N'-Tetramethylethylenediamine → 2-[Bis(tricyclo[3.3.1.13,7]dec-1-yl)phosphino]-1-phenyl-1H-pyrrole

https://huagongshe.com/ko/reaction/732876

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물1-PhenylpyrroleHCID 12480—
반응물Di-1-adamantylchlorophosphineHCID 11110495—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매HexaneHCID 8058—
생성물2-[Bis(tricyclo[3.3.1.13,7]dec-1-yl)phosphino]-1-phenyl-1H-pyrroleHCID 12186773—

반응 조건

온도60 °C

반응 단계

1.6 ml of TMEDA (15 mmol.) are added to a suspension of 1.43 g (10 mmol.) of N-phenylpyrrole 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, 3.36 g (10 mmol.) of di-1-adamantylchlorophosphane are mixed with 40 ml of hexane and heated to 76° C. (solution 2). The boiling solution 1 is then slowly transferred into solution 2, which is at 76° C., by means of a cannula. The mixture is then boiled for a further 2 hours at reflux, the solution is cooled, and 20 ml of water are added thereto. The organic phase is filtered off over magnesium sulfate. The solution is concentrated in vacuo; 15 ml of toluene are added thereto, and the mixture is heated to 60° C. and then cooled. After one day at room temperature, the product is filtered off. Yield: 3.3 g (75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589081B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-2e2e1e695dd84700a40876b63117ff6e
출처 메모uspto-grants-2009_09