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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432830생성일: 2026년 10월 26일

Benzaldehyde → (S)-ethyl 1-benzyl-3-piperidinecarboxylate

https://huagongshe.com/reaction/432830

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Ethyl (3S)-piperidine-3-carboxylateHCID 187784—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물(S)-ethyl 1-benzyl-3-piperidinecarboxylateHCID 76347939.5%

반응 단계

(S)-ethyl nipecotate (309.1 mg; 1.97 mmol) was dissolved in anhydrous methanol (8 ml) and commercially available benzaldehyde (200 μl; 1.97 mmol) was added, followed by sodium cyanoborohydride (234 mg; 3.72 mmol). This mixture was allowed to stir at ambient temperature for 23 hours and was then diluted with dichloromethane. The dichloromethane was washed with water, then washed with saturated sodium chloride solution, dried with anhydrous potassium carbonate, and evaporated under reduced pressure at ambient temperature. The crude product was purified by chromatography on silica eluting with 50% ethyl acetate/50% hexane, giving (S)-ethyl 1-benzyl-3-piperidinecarboxylate (192.7 mg) as a colorless oil. MS mi/z (positive ion) 248 (MH+; 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664271B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-472ed590b85742f8a3342adc795a622e
출처 메모uspto-grants-2003_12