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HRID 962455作成日:2026年10月26日

Hydrochloric Acid → 4-(2-Dimethylaminoethylidene)-1-(2-phenoxyethyl)piperidine dihydrochloride

https://huagongshe.com/reaction/962455

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
反応物1-(2-Phenoxyethyl)-4-piperidoneHCID 18002036—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物4-(2-Dimethylaminoethylidene)-1-(2-phenoxyethyl)piperidine dihydrochlorideHCID 19085461—

反応条件

温度0 °C

反応手順

n-Butyllithium (9.13 ml, 2.5M solution in hexanes) was added to a suspension of (2-dimethylaminoethyl)triphenylphosphonium bromide (9.46 g) in dry THF (60 ml) under nitrogen at 0° C. over 5 minutes. The mixture was stirred at 0° C. for 30 minutes and then 1-(2-phenoxyethyl)-4-piperidone (5.0 g) in THF (15 ml) was added dropwise over 5 minutes. The mixture was warmed to ambient temperature and then heated at 60° C. for 5 hours. The mixture was left at ambient temperature for 18 hours and then quenched with water and diluted with ethyl acetate. 2M Hydrochloric acid was added and the mixture was separated. The organic layer was extracted with 2M hydrochloric acid and the combined acidic layers were basified and extracted with dichloromethane to give an oil. The oil was purified by flash column chromatography on silica using dichloromethane and then dichloromethane/methanol (1:1) as the mobile phase. The oil obtained after chromatography was dissolved in ether and treated with ethereal hydrogen chloride. The ether was decanted off and the residual semi-solid was triturated with acetone/ether (1:1) and filtered to give a solid which was recrystallised from IMS to give 4-(2-dimethylaminoethylidene)-1-(2-phenoxyethyl)piperidine dihydrochloride, m.p. 234°-235° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760035
出典データセットuspto-grants-1998_06
ORD IDord-488fa014f20040eaa53838fb402a9702
出典メモuspto-grants-1998_06