Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfate | HCID 6497 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Bromo-2,6-dimethoxyphenol | HCID 14845876 | — |
| Katalysator | Dimethyl Sulfate | HCID 6497 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-Bromo-1,2,3-trimethoxybenzene | HCID 75885 | 79% |
Reaktionsschritte
A mixture of 74 g (0.32 mol) of 4-bromo-2,6-dimethoxy-phenol 17 and 32 g (0.8 mol) of NaOH in 850 ml of H2O was cooled to 10° C. and 45 ml (0.48 mmol) of dimethyl sulfate was added. The mixture was refluxed for 3 h and an equal amount of dimethyl sulfate (total 0.96 mol) was then added. The mixture was refluxed for another 3 h. Upon cooling overnight, the gray product solidified and was filtered off and dissolved in 1.2 l of ether. The ether solution was filtered to remove insoluble impurity and washed sequentially with 5% NaOH solution (200 ml), water (2×200 mL), and brine (200 mL). The ether phase was dried over Na2SO4 to give a off-white solid, which was recrystallized in hexane (300 ml) to give 62.3 g (79%) of 18.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06653485B2 |
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| Quelldatensatz | uspto-grants-2003_11 |
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| ORD ID | ord-a386ab1999fc4b2fa6f2849a1d9293b1 |
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| Quellennotiz | uspto-grants-2003_11 |
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