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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31654Generated: October 26, 2026

Ethylene Glycol → Ethyl 2-(2-ethyl-1,3-dioxolan-2-yl)acetate

https://huagongshe.com/reaction/31654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl 3-oxovalerateHCID 78656—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductEthyl 2-(2-ethyl-1,3-dioxolan-2-yl)acetateHCID 1424423058.9%

Reaction Steps

A mixture of ethyl 3-oxopentanoate (5 g, 34.7 mmol), ethylene glycol (10.8 g, 174 mmol), triethyl orthoformate (5.14 g, 34.7 mmol), and p-toluenesulfonic acid monohydrate (598 mg, 3.14 mmol) was stirred at room temperature overnight. To the reaction mixture, heptane and ethyl acetate were added to dilute solution, which was washed with water. The organic layer was washed with a saturated saline solution, dried over magnesium sulfate, filtrated and the filtrate was concentrated under reduced pressure. The residue was dissolved in heptane and subjected to NH silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=1/0→10/1) to obtain the title compound (3.85 g, yield: 58.9%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425634B2
Source datasetuspto-grants-2008_09
ORD IDord-0f477811c9694e35a09ec124018f0987
Source noteuspto-grants-2008_09