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HRID 745045作成日:2026年10月26日

1-(4-Nitrobenzoyl)-1,2,3,4-tetrahydroquinoline → (4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanone

https://huagongshe.com/reaction/745045

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Nitrobenzoyl)-1,2,3,4-tetrahydroquinolineHCID 3763693—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物(4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanoneHCID 298411797.8%

反応手順

To a solution of 10% Pd-C (5 g) in ethanol (500 ml) is added 1-(4-nitrobenzoyl)-1,2,3,4-tetrahydroquinoline (53.4 g) and the mixture is subjected to catalytic reduction at ordinary temperature under atmospheric pressure of hydrogen. After the reduction, 10% Pd-C is removed by filtration, and the filtrate is concentrated under reduced pressure to give 1-(4-aminobenzoyl)-1,2,3,4-tetrahydroquinoline (46.7 g) as yellow powder, m.p. 185°-188° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05559230
出典データセットuspto-grants-1996_09
ORD IDord-e8aac1cea9164d018bc289c932d92af7
出典メモuspto-grants-1996_09