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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850357Generated: November 1, 2026

2,2-Diethyl-1,2,3,4-tetrahydro-7-nitroquinoline → 7-Amino-2,2-diethyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/850357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Diethyl-1,2,3,4-tetrahydro-7-nitroquinolineHCID 10513865—
Reactant2,2-Dimethyl-1,2,3,4-tetrahydroquinolin-7-amineHCID 10535287—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product7-Amino-2,2-diethyl-1,2,3,4-tetrahydroquinolineHCID 1072689994%

Reaction Steps

This compound was prepared in a manner similar to that described for 7-amino-1,2,3,4-tetrahydro-2,2-dimethylquinoline (structure 19 of Scheme III, where R1 =R2 =Me) from for 2,2-diethyl-1,2,3,4-tetrahydro-7-nitroquinoline (0.311 g, 1.33 mmol) and 10% Pd/C (31 mg, 10% by weight) in EtOAc (4.0 mL) and EtOH (4.0 mL) to afford 255 mg (94%) of 7-amino-2,2-diethyl-1,2,3,4-tetrahydroquinoline. Data for 7-amino-2,2-diethyl-1,2,3,4-tetrahydroquinoline: Rf 0.26 (4:1 hexanes:ethyl acetate); 1H NMR (400 MHz, CDCl3) 6.77 (d, J=7.9H, 1H), 6.12 (dd, J=7.9, 1.9, 1H), 6.05 (d, J=2.0, 1H), 4.68 (broad s, 3H), 2.62 (t, J=6.7, 2H), 1.67 (t, J=6.7, 2H), 1.38-1.55 (m, 4H), 0.85 (t, J=7.4, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017924
Source datasetuspto-grants-2000_01
ORD IDord-4a6dce061aff4e38bc2cb20cf1089f2a
Source noteuspto-grants-2000_01