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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1669642Erstellt: 25. Oktober 2026

Phenol → 4,4'-[4-(Trifluoromethyl)cyclohexane-1,1-diyl]diphenol

https://huagongshe.com/reaction/1669642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
Edukt4-(Trifluoromethyl)cyclohexanoneHCID 2777491—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt4,4'-[4-(Trifluoromethyl)cyclohexane-1,1-diyl]diphenolHCID 67333442—

Reaktionsschritte

A solution of 4-(trifluoromethyl)cyclohexanone (1.13 g, 6.8 mmol) and phenol (2.01 g, 21.4 mmol) in 3 mL of concentrated HCl (aq) was stirred at 40° C. for 18 h. The reaction mixture was diluted with EtOAc and saturated aqueous NaHCO3 was slowly added. The organic layer was collected and the aqueous layer was extracted twice with EtOAc. The combined organic layers were concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with a gradient of 0% to 40% EtOAc/hexanes over 10 column volumes, then 40% to 100% EtOAc/hexanes over 5 column volumes, affording the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07989472B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-66dcd8f751764dc8aef01be8a59c9e70
Quellennotizuspto-grants-2011_08