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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032056생성일: 2026년 10월 27일

Novoldiamine → 1,3-Bis[[p-(dimethylamino) benzylidene]amino]-2-[[4-(diethylamino)-1-methylbutyl]amino]imidazolium tetrafluoroborate

https://huagongshe.com/reaction/1032056

반응식

참여 물질

역할이름HCID투입량
반응물NovoldiamineHCID 78953—
반응물1,3-Bis[[p-(dimethylamino)benzylidene]amino]-2-(methylthio)imidazolium tetrafluoroborateHCID 73867526—
용매AcetonitrileHCID 6342—
생성물1,3-Bis[[p-(dimethylamino) benzylidene]amino]-2-[[4-(diethylamino)-1-methylbutyl]amino]imidazolium tetrafluoroborateHCID 73771008—

반응 단계

2.47 g of 1,3-bis[[p-(dimethylamino)benzylidene]amino]-2-(methylthio)imidazolium tetrafluoroborate are suspended in 50 ml of absolute acetonitrile, whereupon the suspension is treated with 7.8 g of absolute 2-amino-5-(diethylamino)pentane. The mixture is stirred at room temperature under an argon atmosphere for about 24 hours. The insoluble constituents are removed by filtration and the filtrate is treated with 450 ml of diethyl ether. The pale yellow precipitate obtained is removed by filtration under suction, washed three times with diethyl ether and recrystallized from methanol/diethyl ether. There is obtained pale yellow 1,3-bis[[p-(dimethylamino) benzylidene]amino]-2-[[4-(diethylamino)-1-methylbutyl]amino]imidazolium tetrafluoroborate of melting point 187°-191° (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04956470
출처 데이터셋uspto-grants-1990_09
ORD IDord-ec3f271a912c42e2968aad8e48d1cbd2
출처 메모uspto-grants-1990_09