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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1637981Erstellt: 25. Oktober 2026

Bisphenol A → 2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propane

https://huagongshe.com/reaction/1637981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBisphenol AHCID 6623—
EduktEpichlorohydrinHCID 7835—
EduktSodium HydroxideHCID 14798—
Edukt2-ButyloxiraneHCID 15036—
KatalysatorBenzyltrimethylammonium bromideHCID 21449—
KatalysatorTetramethylammonium bromideHCID 66137—
LösungsmittelWaterHCID 962—
Produkt2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propaneHCID 22600643—

Reaktionsschritte

With stirring, 100.2 g (1 mol) of butyl oxirane, 114 g (0.5 mol) of bisphenol A and 2.14 g of benzyltrimethylammonium bromide are heated to 110° C. When the exothermic reaction has subsided (rise in temperature to 115° C.), the reaction is further stirred at 110° C. until the epoxy value is less than 0.1 eq/kg (16 h). 85.52 g (0.2 mol) of the resultant reaction product are reacted with 296 g (3.2 mol) of epichlorohydrin and 1.32 g of tetramethylammonium bromide according to the method described in EP-A 22 073. After addition of 33.6 g (0.42 mol) of 50% aqueous sodium hydroxide and removal of the water under vacuum, the product is isolated and dried.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06043323
Quelldatensatzuspto-grants-2000_03
ORD IDord-79f00eda87254d118b386ac11fba9a99
Quellennotizuspto-grants-2000_03