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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218900Generated: October 27, 2026

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

https://huagongshe.com/reaction/2218900

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 numberUS07410971B2
Source datasetuspto-grants-2008_08
ORD IDord-86f35078472841049f3d476a88959631
Source noteuspto-grants-2008_08