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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483856Erstellt: 25. Oktober 2026

Hydrochloric Acid → (1,1'-Biphenyl)-2,3'-diol

https://huagongshe.com/reaction/483856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhenolHCID 996—
Edukt1-DodecanethiolHCID 8195—
Edukt3,3,5-TrimethylcyclohexanoneHCID 13398—
EduktSodium HydroxideHCID 14798—
LösungsmittelWaterHCID 962—
Produkt(1,1'-Biphenyl)-2,3'-diolHCID 33665—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

1692 g (18 mol) of phenol, 60.6 g (0.3 mol) of dodecylthiol and 420 g (3 mol) of dihydroisophorone (3,3,5-trimethylcyclohexan-1-one) are introduced into a stirring apparatus equipped with a stirrer, thermometer, reflux condenser and gas inlet pipe at 28°-30° C. Dry HCl gas is introduced into this solution over a period of 5 hours at 28°-30° C. The mixture is then left to react for about 10 h at 28°-30° C. When 95% of the ketone has been converted (examined by GC), 2.5 l of water are added to the reaction mixture and a pH value of 6 is adjusted by adding a 45% NaOH solution. The reaction mixture is stirred for one hour at 80° C. and then cooled to 25° C. The aqueous phase is decanted off and the remaining residue is washed with water at 80° C. The resulting crude product is filtered off and hot-extracted twice with n-hexane and twice with methylene chloride and then filtered. The residue is recrystallised twice from xylene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05227458
Quelldatensatzuspto-grants-1993_07
ORD IDord-44d3854980e7474cabb4290501e38724
Quellennotizuspto-grants-1993_07