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Ethylene Oxide → 3-Phenoxy-1,2-propanediol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylene Oxide | HCID 6354 | — |
| 反応物 | Phenothiazine | HCID 7108 | — |
| 反応物 | Phenyl glycidyl ether | HCID 31217 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 触媒 | Tetrapropylammonium bromide | HCID 74745 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 3-Phenoxy-1,2-propanediol | HCID 10857 | — |
反応手順
A solution of 150.2 g. phenyl glycidyl ether (1.0 eq.), 200.0 g. AOnPA (1.15 eq., of Example 1), 200.0 g. toluene, 4.0 g. tetrapropylammonium bromide (0.015 eq.), and 1.0 g. phenothiazine was heated at reflux for 6.0 hours. Conversion, measured by residual oxirane titer, was ca. 93%. Upon cooling, the reactor was charged with 186.0 g. of the AOnPA (1.07 eq.), 150.0 g. toluene, and 10.0 g. p-toluenesulfonic acid monohydrate (0.05 eq.). The mixture was again heated at reflux. After 6.0 hrs., conversion was 90%. The product was extracted with ether and purified by washing. It had an acrylate titer of 3.8 meq./g. (theory: 4.17 meq./g.) and Brookfield viscosity of 230 centipoise at 25° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05243069 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-167fda6db42f40c2b04d4c02c0deb86d |
| 出典メモ | uspto-grants-1993_09 |