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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850346Generated: October 31, 2026

Ethanol → 2,2-Dimethyl-1,2,3,4-tetrahydroquinolin-7-amine

https://huagongshe.com/reaction/850346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,2,3,4-Tetrahydro-2,2-dimethyl-7-nitroquinolineHCID 10512465—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2,2-Dimethyl-1,2,3,4-tetrahydroquinolin-7-amineHCID 1053528799.6%

Reaction Steps

In a 200-mL r.b. flask, a solution of 1,2,3,4-tetrahydro-2,2-dimethyl-7-nitroquinoline (1.00 g, 4.84 mmol) in 1:1 EtOH:EtOAc (40 mL) was treated with 10% Pd/C (0.20 g). The reaction mixture was de-gassed and fitted with a balloon of H2. The reaction mixture was stirred for 6 h, de-gassed, and filtered through a pad of Celite. The pad was rinsed with EtOAc (300 mL). The filtrate was concentrated to afford 0.85 g (99%) of the crude aniline as a reddish oil. Data for 7-amino-1,2,3,4-tetrahydro-2,2-dimethylquinoline: 1H NMR (400 MHz, CDCl3) 6.77 (d, J=7.9, 1H), 6.00 (dd, J=7.9, 2.2, 1H), 5.81 (d, J=2.2, 1H), 3.47 (bs, 1H), 3.40 (bs, 2H), 2.66 (t, J=6.7, 2H), 1.65 (t, J=6.7, 2H), 1.18 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017924
Source datasetuspto-grants-2000_01
ORD IDord-ac82240be7af48e1b0ca291eeb859166
Source noteuspto-grants-2000_01