HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418890Erstellt: 26. Oktober 2026
Dimethyl dicarbonate → 2,3,3',4'-Tetramethylbenzophenone
https://huagongshe.com/reaction/418890
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl dicarbonate | HCID 3086 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3,4-Dimethylbenzoic acid | HCID 12073 | — |
| Edukt | 2,3-Dimethylphenylboronic acid | HCID 2773395 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2,3,3',4'-Tetramethylbenzophenone | HCID 20372118 | 42% |
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 as 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093348B1 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-40f67c7c6ebe4f6fa1f0e5363b4b4569 |
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| Quellennotiz | uspto-grants-2012_01 |
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