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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5244Generated: October 26, 2026

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

https://huagongshe.com/reaction/5244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantPhenothiazineHCID 7108—
ReactantPhenyl glycidyl etherHCID 31217—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
CatalystTetrapropylammonium bromideHCID 74745—
SolventTolueneHCID 1140—
Product3-Phenoxy-1,2-propanediolHCID 10857—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05243069
Source datasetuspto-grants-1993_09
ORD IDord-167fda6db42f40c2b04d4c02c0deb86d
Source noteuspto-grants-1993_09