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HRID 1830724作成日:2026年10月27日

Benzaldehyde → N-benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1830724

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物4-PiperidinecarboxamideHCID 3772—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-benzylpiperidine-4-carboxamideHCID 386806451.7%

反応手順

To a suspension of isonipecotamide (12.3 g, 96 mmol) in 200 mL of dichloromethane, was added, benzaldehyde (10.6 g, 100 mmol) and sodium triacetoxyborohydride (29.7 gm, 140 mmol) and the mixture was stirred at room temperature for 5 days. The thick white mixture was diluted with 100 mL water and extracted with EtOAc (2×20 mL). The aqueous phase was basified with 1N NaOH to pH>12. The resulting white precipitate was collected by suction filtration. The white solid was subsequently taken up in 50 mL of EtOAc, and was washed with 20 mL of brine, then dried (MgSO4), filtered and concentrated to give 10.84 g (50%) of the desired product. 1H-NMR (400 MHz, CDCl3) δ7.85 (m, 5H), 5.45 (s, 1H), 5.34 (s, 1H), 3.5 (s, 2H), 2.93 (d, J=10.96 Hz, 2H), 2.16 (t, J=12.13 Hz, 1H), 2.01 (t, J=11.74 Hz, 2H), 1.87 (d, J=12.52 Hz, 2H), 1.76 (q, J=12.52 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07067506B2
出典データセットuspto-grants-2006_06
ORD IDord-b6e5831158794da89645e89ab4cd8afb
出典メモuspto-grants-2006_06