Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2,4-Di-tert-pentylphenol | HCID 8455 | — |
| Edukt | Heptane | HCID 8900 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Methyl 2-bromo-5-methoxybenzoate | HCID 2776849 | — |
| Katalysator | Cuprous chloride | HCID 62652 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 19373458 | HCID 19373458 | 90% |
Reaktionsschritte
To a solution of sodium hydride (1.2 g, 0.05 mol) in pyridine (60 mL), was added a solution of 2,4-di-tert-pentylphenol (12.9 g, 0.055 mol) in pyridine (20 mL) with stirring. Gas evolution ceased in approximately 1.5 hr at which time methyl 2-bromo-5-methoxylbenzoate was added. Copper (I) chloride (1.24 g, 0.0126 mol) was added and the mixture heated to reflux for 8 hours. The reaction mixture was diluted with diethyl ether (100 mL) and washed with 3N HCl (3×50 mL) and then washed with saturated sodium bicarbonate (1×50 mL). The organic extracts were dried over sodium sulfate, filtered and concentrated to give a dark oil. Chromatography on silica gel with 1:1 heptane:ethyl acetate yielded the pure product as a viscous oil in 90% yield. NMR and mass spectral analysis were consistent with proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05258407 |
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| Quelldatensatz | uspto-grants-1993_11 |
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| ORD ID | ord-26886d3d31674d648fabaee48036271f |
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| Quellennotiz | uspto-grants-1993_11 |
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