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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815741생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane

https://huagongshe.com/reaction/1815741

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Potassium CarbonateHCID 11430—
반응물1,3-DiiodopropaneHCID 12314—
반응물1,4,7-TriazacyclononaneHCID 188318—
반응물4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
용매AcetonitrileHCID 6342—
생성물4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
생성물HCID 17939386HCID 17939386—

반응 단계

N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-bis[N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluene-sulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19). 1.1.22 1,4,7,10-Tetraazabicyclo[5.5.2]tetradecane

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06881732B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-40ea47cb16174880a641f1495dd0ae66
출처 메모uspto-grants-2005_04