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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1742121Erstellt: 26. Oktober 2026

Phenol → BPTMC phenol

https://huagongshe.com/reaction/1742121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
Edukt3,3,5-TrimethylcyclohexanoneHCID 13398—
Edukt4,4'-(3,3,5-Trimethylcyclohexylidene)bis(phenol)HCID 4134035—
LösungsmittelWaterHCID 962—
ProduktBPTMC phenolHCID 70193612—

Reaktionsschritte

In a method of making 1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane in the form of an adduct with phenol wherein 3,3,5-trimethylcyclohexanone is reacted with phenol in the presence of an acid condensation catalyst and an alkane thiol of the formula R1R2CHSH where R1 is an alkyl, aryl or alkaryl group having from 1 to about 20 carbon atoms and R2 is H or R1, to obtain a reaction mixture including 1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane in the form of an adduct with phenol, the improvement comprising adding water to said reaction mixture to obtain a slurry, filtering said slurry to obtain 1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane phenol adduct as a solid, and a filtrate having an organic phase and an aqueous phase, recovering said organic phase, contacting said organic phase with an acid condensation catalyst at a temperature of about 0° C. to about 150° C., and adding phenol and 3,3,5-trimethylcyclohexanone to the organic phase so treated to make additional 1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05336812
Quelldatensatzuspto-grants-1994_08
ORD IDord-3b82b8dc5ce54e2faa073b229187a6e0
Quellennotizuspto-grants-1994_08