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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963319생성일: 2026년 10월 26일

Methyl Methanesulfonate → 1-Methyl-3-[3-[4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridinium methanesulfonate

https://huagongshe.com/reaction/963319

반응식

참여 물질

역할이름HCID투입량
반응물Methyl MethanesulfonateHCID 4156—
반응물3-[3-[4-(5-Trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridineHCID 19082012—
용매DichloromethaneHCID 6344—
생성물1-Methyl-3-[3-[4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridinium methanesulfonateHCID 19082040157%

반응 단계

To a solution of 3-[3-[4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridine (1 g, 2.6 mmol, 1.1 eq) in 10 ml of methylene chloride was added methyl methanesulfonate (0.32 g, 2.9 mmol) and the mixture was gently refluxed overnight. After adding 0.5 eq of methyl methanesulfonate, the mixture was allowed to reflux an additional 24 h. The mixture was concentrated in vacuo and a solid residue was washed with ether to afford 1.11 g (85.3%) of 1-methyl-3-[3-[4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridinium methanesulfonate, as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763461
출처 데이터셋uspto-grants-1998_06
ORD IDord-be7cb0573eb543ca967f7964071715cc
출처 메모uspto-grants-1998_06