Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291606Generated: October 25, 2026

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

https://huagongshe.com/reaction/1291606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrobenzoyl)-1,2,3,4-tetrahydroquinolineHCID 3763693—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
Product(4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanoneHCID 298411797.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753677
Source datasetuspto-grants-1998_05
ORD IDord-f8eb297d32cf49bdb3e8e15ac710971e
Source noteuspto-grants-1998_05