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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 4-(10-Bromodecyloxy)-4'-dodecylazobenzene | HCID 19792929 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 10-[4-[[4-(dodecyl)phenyl]azo]phenoxy]-N-(2-hydroxyethyl)-N,N-dimethyl-1-decanaminium bromide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05246747 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-1d8e39248edc4f098a636d77133a05dd |
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| 출처 메모 | uspto-grants-1993_09 |
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