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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604392생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/604392

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물PiperidineHCID 8082—
반응물Potassium CarbonateHCID 11430—
반응물5-ChlorovaleronitrileHCID 80474—
반응물Aluminium lithium hydrideHCID 21226445—
반응물HCID 86594854HCID 86594854—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-(Piperidin-1-yl)pentan-1-amineHCID 713844759%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910605B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-a848a1a768d44709b5ed7825f960b825
출처 메모uspto-grants-2011_03