化工社化工社 化学情報印刷レポート · 研究参考用
Bisphenol A → 2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Bisphenol A | HCID 6623 | — |
| 反応物 | Epichlorohydrin | HCID 7835 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Butyloxirane | HCID 15036 | — |
| 触媒 | Benzyltrimethylammonium bromide | HCID 21449 | — |
| 触媒 | Tetramethylammonium bromide | HCID 66137 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2,2-Bis[p-(2-glycidyloxyhexoxy)phenyl]propane | HCID 22600643 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06043323 |
| 出典データセット | uspto-grants-2000_03 |
| ORD ID | ord-79f00eda87254d118b386ac11fba9a99 |
| 出典メモ | uspto-grants-2000_03 |