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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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl BromideHCID 6323—
반응물2-(Methylamino)ethanolHCID 8016—
반응물1-[N-Methyl-N-(2-hydroxyethyl)amino]-3-(12-hydroxyoctadecyl)-2-propanolHCID 19694598—
반응물N-(3-methoxy-2-hydroxy-propyl)-N-methyl-2-hydroxyethylamineHCID 19694612—
반응물12-Hydroxyoctadecyl glycidyl etherHCID 19694653—
용매Diethyl EtherHCID 3283—
생성물N-(2-hydroxypropyl)-N,N-dimethyl-N-[3-(12-hydroxyoctadecyl)-2-hydroxypropyl]ammonium bromideHCID 1969460390%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723497
출처 데이터셋uspto-grants-1998_03
ORD IDord-540e2d8dfa8f4e3c817851023a8dc240
출처 메모uspto-grants-1998_03