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HRID 1814855作成日:2026年10月27日

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

https://huagongshe.com/reaction/1814855

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US06878713B2
出典データセットuspto-grants-2005_04
ORD IDord-a38b431759e645758c14daa8fa0f3cf1
出典メモuspto-grants-2005_04