돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5755생성일: 2026년 10월 23일

2-(Dimethylamino)ethanol → 10-[4-[[4-(dodecyl)phenyl]azo]phenoxy]-N-(2-hydroxyethyl)-N,N-dimethyl-1-decanaminium bromide

https://huagongshe.com/ko/reaction/5755

반응식

참여 물질

역할이름HCID투입량
반응물2-(Dimethylamino)ethanolHCID 7902—
반응물TetrahydrofuranHCID 8028—
반응물4-(10-Bromodecyloxy)-4'-dodecylazobenzeneHCID 19792929—
용매MethanolHCID 887—
생성물10-[4-[[4-(dodecyl)phenyl]azo]phenoxy]-N-(2-hydroxyethyl)-N,N-dimethyl-1-decanaminium bromideHCID 19792927—

반응 단계

A 3000 ml three-necked round bottom flask was equipped with magnetic stirring, a heating mantle, a reflux condenser, and a nitrogen atmosphere. The flask was charged with 4-(10-bromodecyloxy)-4'-dodecylazobenzene (40 g, 0.068 mol), dimethylethanolamine (95.2 g, 1.068 mole) and 1050 ml of tetrahydrofuran. The reaction mixture was allowed to reflux for 24 hours. During the course of the reaction mixture. After 24 hours, the reaction mixture was cooled to room temperature, and then chilled in an icewater bath. The crystalline solid was isolated by suction filtration. The crude product was dissolved in hot methanol and filtered to remove insoluble impurities. The methanol was removed by evaporation at reduced pressure The crude product was recrystallized from tetrahydrofuran. Yield 28.0 g, 61.0%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246747
출처 데이터셋uspto-grants-1993_09
ORD IDord-1d8e39248edc4f098a636d77133a05dd
출처 메모uspto-grants-1993_09