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HRID 604392作成日:2026年10月25日

Potassium Iodide → 5-(Piperidin-1-yl)pentan-1-amine

https://huagongshe.com/reaction/604392

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物PiperidineHCID 8082—
反応物Potassium CarbonateHCID 11430—
反応物5-ChlorovaleronitrileHCID 80474—
反応物Aluminium lithium hydrideHCID 21226445—
反応物HCID 86594854HCID 86594854—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-(Piperidin-1-yl)pentan-1-amineHCID 713844759%

反応手順

5-Chlorovaleronitrile (10 mmol), 20 mmol of piperidine, 20 mmol of potassium carbonate and a catalytic amount of potassium iodide in 50 ml of ethanol were refluxed for 6 hours. The solvent was removed under reduced pressure, the residue suspended in water and extracted with methylene chloride. The organic layer was purified by column chromatography on silica gel using methylene chloride/methanol/aqueous ammonia (90/10/1) as eluent (Yield: 59%). The product was added dropwise to a suspension of 25 mmol of lithium aluminium hydride in 25 ml of dry tetrahydrofurane at 0° C. After refluxing for 1 hour 10 ml of a saturated solution of sodium/potassium tartrate in water was added dropwise. The residue was filtered off and the filtrate purified by column chromatography on silica gel using methylene chloride/methanol/aqueous ammonia (90/10/1) as eluent. The residue was crystallized with hydrochloric acid from diethyl ether/2-propanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910605B2
出典データセットuspto-grants-2011_03
ORD IDord-a848a1a768d44709b5ed7825f960b825
出典メモuspto-grants-2011_03