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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258212Erstellt: 26. Oktober 2026

tert-Butanol → Phenol, 2-(1,1-dimethylethyl)-4-(1,1,3,3-tetramethylbutyl)-

https://huagongshe.com/reaction/258212

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
Edukt4-Tert-octylphenolHCID 8814—
LösungsmittelWaterHCID 962—
LösungsmittelTrifluoroacetic acidHCID 6422—
ProduktPhenol, 2-(1,1-dimethylethyl)-4-(1,1,3,3-tetramethylbutyl)-HCID 60557354%

Reaktionsschritte

4-t-octylphenol (160 g, 0.78 mole) was dissolved in 400 ml anhydrous TFA. T-butyl alcohol (94.3 g, 1.27 mole) was added with stirring. The mixture was stoppered and stirred for 24 hours at ambient (~22° C.) temperature. This solution was diluted with 600 ml water, and the resulting upper organic layer was isolated in a separatory funnel. The crude product, 2-t-butyl-4-t-octylphenol, was dried over anhydrous magnesium sulfate and purified by eluting 35 g of the mixture with 70:30 hexanes:dichloromethane (v/v) in a 5×20 cm silica column, then eluted with 300 to 700 ml of solvent and collected in aliquots of 50 ml. Aliquots showing a single spot by TLC on silica eluted with 70:30 hexanes:dichloromethane (v/v) were combined and rotoevaporated to a thick syrup for a yield of 54%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05266283
Quelldatensatzuspto-grants-1993_11
ORD IDord-843e434730ac4e9cbf0db26c285ece4a
Quellennotizuspto-grants-1993_11