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HRID 238268作成日:2026年10月27日

Ammonium formate → Tert-butyl 4-(2-cyanophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/238268

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物tert-butyl 4-(2-cyanophenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 18326592—
触媒PalladiumHCID 23938—
溶媒WaterHCID 962—
生成物Tert-butyl 4-(2-cyanophenyl)piperidine-1-carboxylateHCID 1832658574.5%

反応手順

4-(2-Cyano-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (0.2 g) was dissolved in IMS (15 mL) and palladium on carbon (10%; 0.08 g) in water (0.5 mL) was added. Ammonium formate (0.3 g) was added and the mixture heated at reflux for 0.5 hour. The mixture was allowed to cool, filtered and the solvent removed by evaporation to give the title compound as a clear colourless oil (0.15 g). LCMS m/z 287.3[M+H]+. R.T.=4.63 min (Analytical Method 4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642621B2
出典データセットuspto-grants-2014_02
ORD IDord-6c6b8b24a291417584e13c73563824ae
出典メモuspto-grants-2014_02