Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
Reaktionsschritte
A 1000 mL three-neck, round-bottom flask was equipped with a mechanical stirrer, a pressure-compensating dropping funnel, and a reflux condenser. A nitrogen gas flow adapter with overpressure valve was attached on top of the reflux condenser. A slight nitrogen flow guaranteed an inert gas atmosphere in the apparatus. The flask was charged with 181 g triphenylphosphine (690 mmol) and 160 mL acetonitrile (HPLC grade). The white suspension was cooled in an ice bath for 15 minutes. While stirring, dropwise addition of 101.5 g bromine (635 mmol) took place within 40 minutes. After bromine addition, the ice bath was removed. 124 g of 3,5-di-tertbutylphenol (601 mmol) and 140 mL acetonitrile were added in one portion. The orange/white suspension converted into an orange solution upon heating. The mechanical stirrer was replaced by an egg-shape stir bar. The solution was stirred at gentle reflux temperature for three hours.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06376412B1 |
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| Quelldatensatz | uspto-grants-2002_04 |
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| ORD ID | ord-8a4721adaa65478f8561016645ae4af0 |
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| Quellennotiz | uspto-grants-2002_04 |
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