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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761738Generated: November 1, 2026

Ethanol → 2-(Phenylmethoxy)-1,3-propanediol

https://huagongshe.com/reaction/1761738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactant5-(Benzyloxy)-2-phenyl-1,3-dioxaneHCID 263083—
SolventTolueneHCID 1140—
Product2-(Phenylmethoxy)-1,3-propanediolHCID 20356781.1%

Reaction Steps

A mixture of about 338 g of 5-(benzyloxy)-2-phenyl-m-dioxane, about 1500 ml of ethanol, about 500 ml of water and about 20 ml of sulfuric acid was refluxed for about 2 hours. The ethanol was removed, the acid neutralized with solid bicarbonate, the mixture steam distilled to remove benzaldehyde and then saturated with potassium carbonate. This mixture was extracted three times with ether. The ether extracts were combined, dried and evaporated. Toluene was added and evaporated. The residue was distilled via a Kugelrohr (about 0.1 mm, 170° C.) giving an oil. This oil was dissolved in about 300 ml of toluene, cooled and diluted with two volumes of petroleum ether. Refrigeration produced about 184.69 g of the desired title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04827011
Source datasetuspto-grants-1989_05
ORD IDord-510b45eb10f2424a975d12f83c82798b
Source noteuspto-grants-1989_05