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HRID 1193550作成日:2026年10月26日

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

https://huagongshe.com/reaction/1193550

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2,5-DifluoronitrobenzeneHCID 67767—
反応物4-Ethynyl-1-methylpiperidin-4-olHCID 1419099—
反応物Methane, sulfinylbis-, ion(1-), sodiumHCID 10154010—
溶媒Dimethyl SulfoxideHCID 679—
生成物N-Methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidineHCID 1428148354%

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04810792
出典データセットuspto-grants-1989_03
ORD IDord-115ef21ea1824b1c9100e3f018ca65c2
出典メモuspto-grants-1989_03