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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32256Generated: October 26, 2026

1,2-Dimethoxyethane → 1-Methoxy-4-methyl-2-(3,3,5,5-tetramethylcyclohex-1-enyl)benzene

https://huagongshe.com/reaction/32256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(2-Methoxy-5-methylphenyl)boronic acidHCID 2773485—
Reactant3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflateHCID 11087380—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product1-Methoxy-4-methyl-2-(3,3,5,5-tetramethylcyclohex-1-enyl)benzeneHCID 2314267664.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 2-methoxy-5-methylphenylboronic acid (1 g, 6.02 mmol), trifluoromethanesulfonic acid 3,3,5,5-tetramethylcyclohex-1-enyl ester (1.9 g, 6.62 mmol) produced in Example (4a) and 1,2-dimethoxyethane (30 mL) were added tetrakis(triphenylphosphine)palladium(0) (0.35 g, 0.30 mmol) and 2N aqueous solution of sodium carbonate (9.0 mL, 18.0 mmol), followed by stirring for 3 hours at an external temperature of 90° C. under a nitrogen atmosphere. Brine was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtrated, the resultant filtrate was concentrated under reduced pressure to give a residue, which was purified by silica gel column chromatography (ethyl acetate/heptane) to give 1.0 g of the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425554B2
Source datasetuspto-grants-2008_09
ORD IDord-77dc1dbde4074c49be33a8a4e9f38c52
Source noteuspto-grants-2008_09