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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1193550생성일: 2026년 10월 26일

Sodium hydride → N-Methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine

https://huagongshe.com/reaction/1193550

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,5-DifluoronitrobenzeneHCID 67767—
반응물4-Ethynyl-1-methylpiperidin-4-olHCID 1419099—
반응물Methane, sulfinylbis-, ion(1-), sodiumHCID 10154010—
용매Dimethyl SulfoxideHCID 679—
생성물N-Methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidineHCID 1428148354%

반응 단계

To a stirred solution of dimsyl sodium prepared from 43.0 g of sodium hydride (50% in oil, washed three times with hexanes) and 1100 ml of dimethylsulfoxide was added, in aliquots, 125 g of N-methyl-4-ethynyl-4-piperidinol at a rate such that the temperature remained below 23°. When the addition was complete, 167 g of 2,5-difluoronitrobenzene was added slowly dropwise at a rate such that the temperature remained below 21°. When the addition was complete, the mixture was poured into ice, extracted twice with ether, washed with saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and the filtrate was concentrated. The residue was filtered through 800 g of silica gel (70-250 mesh) and eluted with 3 l of 10% methanol/dichloromethane. Evaporation of solvent provided an oil, which crystallized on standing to yield 134 g (54%) of product. Recrystallization from cyclohexane provided the analytical sample, mp 70°-73°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04810792
출처 데이터셋uspto-grants-1989_03
ORD IDord-115ef21ea1824b1c9100e3f018ca65c2
출처 메모uspto-grants-1989_03