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HRID 463324作成日:2026年10月26日

4'-Fluoroacetophenone → 4-(4-Acetylphenoxy)piperidine oxalate

https://huagongshe.com/reaction/463324

反応式

関与物質

役割名称HCID仕込み量
反応物4'-FluoroacetophenoneHCID 9828—
反応物Sodium hydrideHCID 24758—
反応物OxalateHCID 71081—
反応物Piperidin-4-olHCID 79341—
反応物Methane, sulfinylbis-, ion(1-), sodiumHCID 10154010—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物4-(4-Acetylphenoxy)piperidine oxalateHCID 13457428—

反応手順

To a stirred solution of dimsyl sodium, prepared from 43.2 g of NaH (0.90 mol; 50% in oil, washed 3 times with hexane) and 1200 ml of DMSO was added in aliquots, 100 g (0.989 mol) of 4-hydroxypiperidine such that the temperature remained below 23° (using an ice bath). To the mixture was then added dropwise 120 ml (0.99 mol) of p-fluoroacetophenone. The mixture was then stirred at room temperature overnight, poured into water, extracted twice with ether, washed with saturated sodium chloride and dried over potassium carbonate. Filtration followed by evaporation of the solvent provided an oil. The oil was filtered through 500 g of alumina and eluted 2×500 ml of 5% methanol/ether and 2×500 ml of 10% methanol/ether. The material was contained in fractions 2-4. Evaporation of the solvent provided an oil. The yield of the oxalate was 51.2 g (0.165 mol, 18.4%). Recrystallization from methanol provided analytically pure material, m.p. 183- 187.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04518713
出典データセットuspto-grants-1985_05
ORD IDord-79935b1e181146ab80b6c7d71e76b54d
出典メモuspto-grants-1985_05