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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789999Generated: October 29, 2026

3-Methoxy-2-methylquinoline → 5,6,7,8-Tetrahydro-3-methoxy-2-methylquinoline

https://huagongshe.com/reaction/1789999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-methylquinolineHCID 12820971—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTrifluoroacetic acidHCID 6422—
Product5,6,7,8-Tetrahydro-3-methoxy-2-methylquinolineHCID 2203699399.6%

Reaction Steps

A mixture of 3-methoxy-2-methylquinoline (0.081 mol) in trifluoro-acetic acid (150 ml) was hydrogenated at room temperature under a 34 bar pressure for 48 hours with palladium on activated carbon (2 g) as a catalyst. After uptake of hydrogen (2 equiv.), the catalyst was filtered through celite and washed with H2O. The filtrate was basified with a concentrated NH4 OH solution and extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated, yielding 14.3 g (quant.) of 5,6,7,8-tetrahydro-3-methoxy-2-methylquinoline (interm. 13).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071192B1
Source datasetuspto-grants-2006_07
ORD IDord-e14ca53373f947628d9a61d018702f84
Source noteuspto-grants-2006_07