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HRID 432830作成日:2026年10月26日

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

https://huagongshe.com/reaction/432830

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Ethyl (3S)-piperidine-3-carboxylateHCID 187784—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物(S)-ethyl 1-benzyl-3-piperidinecarboxylateHCID 76347939.5%

反応手順

(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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664271B1
出典データセットuspto-grants-2003_12
ORD IDord-472ed590b85742f8a3342adc795a622e
出典メモuspto-grants-2003_12