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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1709802Erstellt: 24. Oktober 2026

Phenol → 2,4,6-Tris(1-phenylethyl)phenol

https://huagongshe.com/de/reaction/1709802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPhosphoric AcidHCID 1004—
EduktStyreneHCID 7501—
Edukt4-(1-Phenylethyl)phenolHCID 94763—
Edukt2-(1-Phenylethyl)phenolHCID 95322—
Edukt2,4-Bis(1-Phenylethyl)PhenolHCID 102877—
LösungsmittelFormic AcidHCID 284—
Produkt2,4,6-Tris(1-phenylethyl)phenolHCID 86688—
Produkt2,6-Bis(1-phenylethyl)phenolHCID 12236115—

Reaktionsbedingungen

Temperatur110 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04950810
Quelldatensatzuspto-grants-1990_08
ORD IDord-4ffd22c839b0455f9d2fedccbfacbbc6
Quellennotizuspto-grants-1990_08