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HRID 351542作成日:2026年10月27日

Water → HCID 178468978、化合物

https://huagongshe.com/reaction/351542

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物(1,1'-Bicyclohexyl)-4-oneHCID 41690—
反応物Ethyl 4-(piperazin-1-yl)benzoateHCID 2761178—
反応物Sodium cyanoborohydrideHCID 5003444—
触媒Titanium isopropoxideHCID 11026—
溶媒EthanolHCID 702—
生成物HCID 178468978HCID 17846897820.3%

反応手順

A mixture of 4-cyclohexylcyclohexanone (1.54 g), 1-(4-ethoxycarbonylphenyl)piperazine (2 g) and titanium(IV) isopropoxide (3.18 ml) was stirred at room temperature. After 1 hour, the IR spectrum of the mixture showed no ketone band, and the viscous solution was diluted with absolute ethanol (8.5 ml). Sodium cyanoborohydride (0.343 g) was added, and the solution was stirred for 3 hours. Water (3 ml) was added with stirring, and the resulting in organic precipitate was filtered and washed with ethanol. The filtrate was extracted with ethyl acetate. The organic layer was taken and dried over magnesium sulfate. The magnesium sulfate was filtered off, and filtrate was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with (hexane/ethyl acetate)=(3/1). The fractions containing the less polar compound were collected and evaporated under reduced pressure to give ethyl 4-[4-(cis-4-cyclohexylcyclohexyl)piperazin-1-yl]benzoate (692 mg) as byproduct. The fractions containing the more polar compound were collected and evaporated under reduced pressure to give ethyl 4-[4-(trans-4-cyclohexylcyclohexyl)piperazin-1-yl]benzoate (587 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743776B2
出典データセットuspto-grants-2004_06
ORD IDord-9d9de2240edd40cca52a14699746cbfa
出典メモuspto-grants-2004_06