戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1063284作成日:2026年10月25日

Ethylamine hydrochloride → 1-Carbethoxy-4-ethylamino-3-methylpiperidine

https://huagongshe.com/reaction/1063284

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylamine hydrochlorideHCID 11198—
反応物Potassium HydroxideHCID 14797—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Ethyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 15075657—
溶媒MethanolHCID 887—
生成物1-Carbethoxy-4-ethylamino-3-methylpiperidineHCID 22278900—

反応条件

温度0 °C

反応手順

Ethylamine hydrochloride (5 g, 61.34 mmol) was added to the stirred solution of 1-carbethoxy-3-methyl-4-piperidone (3.5 g, 18.9 mmol) obtained as described in Preparation 1, in methanol (30 ml) followed by 3.43 g (61.34 mmol) KOH. Stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (1.4 g, 22.22 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 16 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to give 1-carbethoxy-4-ethylamino-3-methylpiperidine. Yield 2.3 g (54%), C11H22N2O2, m/z 215 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06964966B2
出典データセットuspto-grants-2005_11
ORD IDord-862c9e1624514928a44601e76a9cda7d
出典メモuspto-grants-2005_11