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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52490Generated: October 30, 2026

N-ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinoline → N-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinoline

https://huagongshe.com/reaction/52490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinolineHCID 67722040—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinolineHCID 6772185895%

Reaction Steps

N-Ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinoline (4 g, 12.1 mmol) in ethanol (100 mL) was hydrogenated over 10% palladium on carbon (500 mL) under atmospheric pressure of hydrogen for 1.5 h at room temperature. The mixture was filtered through celite and the filtrate was concentrated to give 3.83 g of N-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinoline (95%): 1H NMR (270 MHz, CDCl3) δ7.03~7.19 (m, 4H), 4.78 (m, 1H), 4.11(q, 4H, J 7 Hz), 2.73 (t, 2H, J=6 Hz), 2.47 (m, 1H), 1.69 (m, 1H), 1.25 (t, 3H, J=7 Hz), 1.11 (t, 3H, J=7Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616586
Source datasetuspto-grants-1997_04
ORD IDord-7587a164b53b4fe89c612e955bd90768
Source noteuspto-grants-1997_04