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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814855생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1814855

반응식

참여 물질

역할이름HCID투입량
반응물Ethylamine hydrochlorideHCID 11198—
반응물Potassium HydroxideHCID 14797—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Ethyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 15075657—
용매MethanolHCID 887—
생성물1-Carbethoxy-4-ethylamino-3-methylpiperidineHCID 22278900—

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06878713B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-a38b431759e645758c14daa8fa0f3cf1
출처 메모uspto-grants-2005_04