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HRID 1943025作成日:2026年10月25日

Ammonia → Tert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1943025

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Tert-butyl 4-(cyano(phenyl)methylene)piperidine-1-carboxylateHCID 44122578—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物Tert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylateHCID 58415947—

反応手順

tert-butyl 4-[cyano(phenyl)methylene]piperidine-1-carboxylate (1.18 g, 3.95 mmol) in ethanol (15 ml) was saturated with NH3 at ambient temperature and Raney nickel (1 ml, 3.95 mmol) in water was added. The reaction was placed on a Parr reactor under H2 pressure (48 psi) for 19 hours. The reaction mixture was then re-saturated with NH3 and additional Raney nickel (1 ml, 3.95 mmol) was added before placing back on the Parr reactor for an additional 5.5 hours. The reaction mixture was filtered through Celite, washing with EtOH, and concentrated in vacuo. The product was carried on without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08389720B2
出典データセットuspto-grants-2013_03
ORD IDord-ab0346fb6807451ebe1ee52b8b17c723
出典メモuspto-grants-2013_03