戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5244作成日:2026年10月23日

Ethylene Oxide → 3-Phenoxy-1,2-propanediol

https://huagongshe.com/ja/reaction/5244

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene OxideHCID 6354—
反応物PhenothiazineHCID 7108—
反応物Phenyl glycidyl etherHCID 31217—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
触媒Tetrapropylammonium bromideHCID 74745—
溶媒TolueneHCID 1140—
生成物3-Phenoxy-1,2-propanediolHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05243069
出典データセットuspto-grants-1993_09
ORD IDord-167fda6db42f40c2b04d4c02c0deb86d
出典メモuspto-grants-1993_09