Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107생성일: 2026년 10월 23일
Methyl Bromide → N-(2-hydroxypropyl)-N,N-dimethyl-N-[3-(12-hydroxyoctadecyl)-2-hydroxypropyl]ammonium bromide
https://huagongshe.com/ko/reaction/1107
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Bromide | HCID 6323 | — |
| 반응물 | 2-(Methylamino)ethanol | HCID 8016 | — |
| 반응물 | 1-[N-Methyl-N-(2-hydroxyethyl)amino]-3-(12-hydroxyoctadecyl)-2-propanol | HCID 19694598 | — |
| 반응물 | N-(3-methoxy-2-hydroxy-propyl)-N-methyl-2-hydroxyethylamine | HCID 19694612 | — |
| 반응물 | 12-Hydroxyoctadecyl glycidyl ether | HCID 19694653 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | N-(2-hydroxypropyl)-N,N-dimethyl-N-[3-(12-hydroxyoctadecyl)-2-hydroxypropyl]ammonium bromide | HCID 19694603 | 90% |
반응 단계
1-[N-Methyl-N-(2-hydroxyethyl)amino]-3-(12-hydroxyoctadecyl)-2-propanol was first prepared from 12-hydroxyoctadecyl glycidyl ether and N-methylethanolamine in the same manner as in the preparation of N-(3-methoxy-2-hydroxy-propyl)-N-methyl-2-hydroxyethylamine in Preparation Example 24. A 200-ml autoclave was charged with 6.3 g (15 mmol) of the thus-prepared compound, 100 ml of diethyl ether and 14.2 g of methyl bromide, and the resultant mixture was stirred at 48° C. for 8 hours. The reaction mixture was then concentrated under reduced pressure, and the resultant residue was dissolved in methanol. Diethyl ether was added to the solution to form crystals. The crystals were collected by filtration, thereby obtaining 6.9 g (yield: 90%) of the title compound (IIb-4).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723497 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-540e2d8dfa8f4e3c817851023a8dc240 |
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| 출처 메모 | uspto-grants-1998_03 |
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