化工社化工社 化学情報印刷レポート · 研究参考用
2,4,6-Tribromophenol → 2,4,6-Tribromophenoxyethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,4,6-Tribromophenol | HCID 1483 | — |
| 反応物 | Ethylene Oxide | HCID 6354 | — |
| 反応物 | Propylene Oxide | HCID 6378 | — |
| 触媒 | Tetramethylammonium chloride | HCID 6379 | — |
| 生成物 | 2,4,6-Tribromophenoxyethanol | HCID 22594837 | — |
反応手順
Monomers of type (e) are prepared by the reaction of 2,4,6--tribromophenol with an alphaolefin oxide such as ethylene oxide and propylene oxide, in the presence of 1 to 3 percent tetramethylammonium chloride at 80° to 100°C. for 3 to 6 hours to form 2,4,6-tribromophenoxyethanol. The reaction mixture is washed thoroughly with water after dissolving in solvent, dried with a drying agent, and stripped of solvent under reduced pressure at 40° to 60°C. The product is then analyzed for hydroxyl number. The yield of this intermediate is generally 40 to 60%. The intermediate is then reacted with maleic anhydride at 80° to 100°C. for 3 to 5 hours to form mono-2,4,6-tribromophenoxyethyl maleate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03932181 |
| 出典データセット | uspto-grants-1976_01 |
| ORD ID | ord-074ca8aac0154b98b241aa824efb5eb5 |
| 出典メモ | uspto-grants-1976_01 |