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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130647Generated: October 26, 2026

Dimethyl dicarbonate → 2,3,3',4'-Tetramethylbenzophenone

https://huagongshe.com/reaction/130647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl dicarbonateHCID 3086—
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-Dimethylbenzoic acidHCID 12073—
Reactant2,3-Dimethylphenylboronic acidHCID 2773395—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2,3,3',4'-TetramethylbenzophenoneHCID 2037211842%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 250 ml 3-necked round-bottom flask, 2,3-dimethylphenylboronic acid (3.6 g. 24 mmol). 3,4-dimethylbenzoic acid (3.0 g. 20 mmol), a selected palladium catalyst (0.6 mmol), dimethyl dicarbonate (2.7 g. 30 mmol) and potassium carbonate (6.22 g. 45 mmol) were mixed with 150 ml of dry dioxane. The reaction mixture was heated at 80° C. overnight to become a viscous reaction mixture. 20 ml of water was added to dissolve the heterogeneous reaction mixture, and dioxane was evaporated to dryness. The aqueous solution was extracted with 20 ml of ethyl acetate, dried over anhydrous magnesium sulfate and then evaporated to dryness. The crude product was purified by silica gel column chromatography eluted by hexane/ethyl acetate=20/80 to afford 2.0 g (33%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381849B1
Source datasetuspto-grants-2008_06
ORD IDord-3be3222c0dbc41d1af544c056c2c0c43
Source noteuspto-grants-2008_06