HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32251Erstellt: 25. Oktober 2026
1,2-Dimethoxyethane → 2-(3,3,5,5-Tetramethylcyclohex-1-enyl)phenol
https://huagongshe.com/reaction/32251
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 2734622 | — |
| Edukt | 3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflate | HCID 11087380 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 2-(3,3,5,5-Tetramethylcyclohex-1-enyl)phenol | HCID 23142526 | 101% |
Reaktionsschritte
To a mixture of 2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenol(3.5 g, 15.9 mmol), trifluoromethanesulfonic acid 3,3,5,5-tetramethylcyclohex-1-enyl ester (5 g, 17.4 mmol) produced in Example (4a) and 1,2-dimethoxyethane (20 mL) were added tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.79 mmol) and 2N aqueous solution of sodium carbonate (23.9 mL, 47.7 mmol), followed by stirring for 1 hour 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 then the solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 3.7 g of the title compound as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425554B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-f1e3eb10a5b247ef95e4208d5352e5da |
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| Quellennotiz | uspto-grants-2008_09 |
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