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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40842생성일: 2026년 10월 24일

Ammonium Acetate → tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/40842

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
용매MethanolHCID 887—
용매Sodium HydroxideHCID 14798—
생성물tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 2264729590%

반응 단계

A mixture of tert-butyl 4-acetylpiperidine-1-carboxylate (145 g, 0.64 mol) and ammonium acetate (225 g, 2.9 mol) in methanol (2 L) was stirred at room temperature for 1.5 hours. Sodium cyanoborohydride (30 g, 0.48 mol) was added in one portion and the stirring was continued overnight at room temperature. The reaction mixture was poured in 2N aq. NaOH (2 L) and extracted with dichloromethane (2×1 L). The combined extracts were washed with water (1 L), brine (0.3 L), and evaporated to dryness. The residue was dissolved in TBME (1.5 L), dried over sodium sulfate, filtered, and evaporated to dryness under reduced pressure. The residue was purified by bulb to bulb distillation at 180° C. and 0.1 mbar to afford the title compound as a colorless oil that partly solidified upon standing (131 g, 90% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530489B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-369371af84394b78a597fa75f03191d5
출처 메모uspto-grants-2013_09