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

HRID 130647

Reaktionsgleichung

[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1B(O)O.[CH3:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[CH3:22])[C:16](O)=[O:17].C(OC(OC)=O)(OC)=O.C(=O)([O-])[O-].[K+].[K+]>[Pd].O1CCOCC1.O>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:16]([C:15]1[CH:19]=[CH:20][C:21]([CH3:22])=[C:13]([CH3:12])[CH:14]=1)=[O:17]

Komponenten

Reaktionsbedingungen

Temperatur: 80 °C

Versuchsvorschrift

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.

Aufarbeitung

customwas evaporated to dryness
extractionThe aqueous solution was extracted with 20 ml of ethyl acetate
dry with materialdried over anhydrous magnesium sulfate
customevaporated to dryness
customThe crude product was purified by silica gel column chromatography
washeluted by hexane/ethyl acetate=20/80

Quellen und Nachweise

ORD-Eintrag: ord-3be3222c0dbc41d1af544c056c2c0c43
Quelldatensatz: uspto-grants-2008_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07381849B1

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