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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050521Generated: October 30, 2026

Methyl iodide → 2-Methoxy-2,4,6-cycloheptatrien-1-one

https://huagongshe.com/reaction/2050521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTropoloneHCID 10789—
ReactantPotassium CarbonateHCID 11430—
ReactantDicyclohexano-18-crown-6HCID 85955—
SolventAcetonitrileHCID 6342—
Product2-Methoxy-2,4,6-cycloheptatrien-1-oneHCID 1654692%

Reaction Steps

To the mixture of 20 g (0.16 mol) of tropolone (2-hydroxy-2,4,6-cycloheptatrienone), 68 g (0.48 mol) of anhydrous potassium carbonate, 6.1 g (0.016 mol) of dicyclohexyl-18-crown-6 and 750 ml of acetonitrile were added 117 g (0.8 mol) of methyl iodide with stirring. After stirred under reflux for 10 hours, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure, and the residue was dissolved in dichloromethane. After washing with 13.8% aqueous solution of potassium carbonate and water. After drying with magnesium sulfate anhydrous, dichloromethane was evaporated under reduced pressure, and the residue was subjected to purification by means of silica gel column chromatography. Elution was carried out by using ethyl acetate and the solvent was evaporated under reduced pressure to give 20 g of 2-methoxytropone (2-methoxy-2,4,6-cycloheptatrienone) (yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013736
Source datasetuspto-grants-1991_05
ORD IDord-361af9dd242f4effbae5e361bbadc82d
Source noteuspto-grants-1991_05