HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Bisphenol A → 2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Bisphenol A | HCID 6623 | — |
| Edukt | Epichlorohydrin | HCID 7835 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Butyloxirane | HCID 15036 | — |
| Katalysator | Benzyltrimethylammonium bromide | HCID 21449 | — |
| Katalysator | Tetramethylammonium bromide | HCID 66137 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06043323 |
| Quelldatensatz | uspto-grants-2000_03 |
| ORD ID | ord-79f00eda87254d118b386ac11fba9a99 |
| Quellennotiz | uspto-grants-2000_03 |