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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243983Generated: October 30, 2026

Dimethyl Sulfate → 6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-7-carbaldehyde

https://huagongshe.com/reaction/1243983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
Reactant6-Methoxy-2-oxo-1,2,3,4-tetrahydro-quinoline-7-carbaldehydeHCID 10125149—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-7-carbaldehydeHCID 10125178—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Methoxy-2-oxo-1,2,3,4-tetrahydro-quinoline-7-carbaldehyde 30 mg (0.146 mmol) was dissolved in 5 ml of anhydrous THF and the solution was cooled to 0° C. The reaction mixture was treated with 16 mg (0.146 mmol) of potassium t-butoxide whereupon it became yellow in color. After stirring for 30 minutes, the mixture was treated with 14 μl (0.146 mmol) dimethylsulfate and slowly warmed to room temperature while stirring for 16 hours. The reaction mixture was diluted with saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate. The organic phase was dried over sodium sulfate and concentrated to an oil. The residue was chromatographed on silica gel eluting with 6/4 ethyl acetate/hexane to afford 16 mg (50%) as a white solid. MS APCI m/e 220 (p+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119207B2
Source datasetuspto-grants-2006_10
ORD IDord-71ee6953a90e4d0db27fa7cb49b7aed4
Source noteuspto-grants-2006_10