戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 887343作成日:2026年10月25日

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

https://huagongshe.com/reaction/887343

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium AcetateHCID 517165—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
溶媒MethanolHCID 887—
溶媒Sodium HydroxideHCID 14798—
生成物tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 2264729590%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08247421B2
出典データセットuspto-grants-2012_08
ORD IDord-1892656c66ba4a8e84e873ddd015b516
出典メモuspto-grants-2012_08