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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130647Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/130647

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl dicarbonateHCID 3086—
EduktPotassium CarbonateHCID 11430—
Edukt3,4-Dimethylbenzoic acidHCID 12073—
Edukt2,3-Dimethylphenylboronic acidHCID 2773395—
KatalysatorPalladiumHCID 23938—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2,3,3',4'-TetramethylbenzophenoneHCID 2037211842%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381849B1
Quelldatensatzuspto-grants-2008_06
ORD IDord-3be3222c0dbc41d1af544c056c2c0c43
Quellennotizuspto-grants-2008_06