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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106575Generated: October 26, 2026

Benzene → 2-Methoxy-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/1106575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantMethyl iodideHCID 6328—
Reactant1,2,5,6,7,8-Hexahydroquinolin-2-oneHCID 264106—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystHCID 178418647HCID 178418647—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-5,6,7,8-tetrahydroquinolineHCID 18180283—

Reaction Steps

A mixture of 5,6,7,8-tetrahydro-2-quinolone [Meyers, A. I. and Garcia-Munoz, G., J. Org. Chem. (1964) 29, 1435] (7.20 g, 48.32 mmol) and silver carbonate (9.33 g, 33.82 mmol) in THF (100 ml)-benzene (20 ml) was treated with methyl iodide (4.67 ml, 10.28 g, 72.48 mmol) and then heated at reflux for 18 h. On cooling to room temperature the mixture was filtered and the filtrate concentrated to give a brown oil which was subjected to column chromatography (silica, hexane-ethyl acetate, 2:1) to afford the title compound (4.40 g) as yellow oil MS (ES+) 164 (MH+). δH (CDCl3) 7,23 (1H, d, J 8.3 Hz), 6.47 (1H, d, J 8.3 Hz), 3.88 (3H, s), 2.78 (2H, t, J 5.9 Hz), 2.65 (2H, t, J 5.9 Hz) and 1.88-1.71 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057329
Source datasetuspto-grants-2000_05
ORD IDord-e1e20ad68861462aa4df92e9f8c78d69
Source noteuspto-grants-2000_05