Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Phosphoric Acid | HCID 1004 | — |
| Edukt | Styrene | HCID 7501 | — |
| Edukt | 4-(1-Phenylethyl)phenol | HCID 94763 | — |
| Edukt | 2-(1-Phenylethyl)phenol | HCID 95322 | — |
| Edukt | 2,4-Bis(1-Phenylethyl)Phenol | HCID 102877 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Produkt | 2,4,6-Tris(1-phenylethyl)phenol | HCID 86688 | — |
| Produkt | 2,6-Bis(1-phenylethyl)phenol | HCID 12236115 | — |
Reaktionsschritte
A four-neck flask with a dropping funnel, a thermometer, a condenser and a stirrer was charged with 5 g of formic acid, 4 g of 85% phosphoric acid and 28 g of phenol, and was heated up to 110° C. Into the reaction mixture was poured 63 g of styrene through a dropping funnel for 3 hours and stirred for an hour. The reaction mixture consisted of 22% of 2-(α-methylbenzyl)phenol, 12% of 4-(α-methylbenzyl)phenol, and 66% of 2,4-di-(α-methylbenzyl)phenol, when analyzed with a gas chromatography as a % area. 2,6-Di-(α-methylbenzyl)phenol and 2,4,6-tri-(α-methylbenzyl)phenol were not formed. Phosphoric acid and acetic acid were removed by washing with water. The organic layer was distilled under reduced pressure at 0.2 mmHg to give 57 g of 2,4-di-(α-methylbenzyl)phenol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04950810 |
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| Quelldatensatz | uspto-grants-1990_08 |
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| ORD ID | ord-4ffd22c839b0455f9d2fedccbfacbbc6 |
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| Quellennotiz | uspto-grants-1990_08 |
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