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HRID 971915Erstellt: 24. Oktober 2026

Methyl 3,5-dichloro-4-hydroxybenzoate → 4,4'-[1,4-Phenylenebis([2,2-dimethyl-1,3-propanediyl]-oxycarbonyl)]bis(2,6-dichlorophenol)

https://huagongshe.com/de/reaction/971915

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3,5-dichloro-4-hydroxybenzoateHCID 76856—
Edukt1,4-Bis(3-hydroxy-2,2-dimethylpropyl)benzeneHCID 20510740—
KatalysatorCalcium AcetateHCID 6116—
KatalysatorStibanalHCID 6327673—
Produkt4,4'-[1,4-Phenylenebis([2,2-dimethyl-1,3-propanediyl]-oxycarbonyl)]bis(2,6-dichlorophenol)HCID 21312585743,8%

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

A mechanically stirred mixture of 0.6 g of calcium acetate, 0.6 g of antimony oxide, 3.75 g (0.15 M) of 1,4-bis(3-hydroxy-2,2-dimethylpropyl)benzene and 132 g (0.6 M) of methyl 3,5-dichloro-4-hydroxybenzoate was heated under nitrogen atmosphere at 200° C. for 18 hours. The reaction mixture was washed three times with benzene in a Waring Blendor and extracted for 5 days with 2 liters of hot benzene. The extract, on cooling, yielded 70 g of 4,4'-[1,4-phenylenebis([2,2-dimethyl-1,3-propanediyl]oxycarbonyl)]bis(2,6-dichlorophenol) melting at 203°-204° C. The infrared spectrum was consistent with the indicated structure. The compound contained 3.185 meq. of OH/g indicating a molecular weight of 628 for the bisphenol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04161607
Quelldatensatzuspto-grants-1979_07
ORD IDord-fd7265c52c7c44f48a36ca0ee8b655d8
Quellennotizuspto-grants-1979_07