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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31685Generated: October 26, 2026

Ethyl ketone → 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane

https://huagongshe.com/reaction/31685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ketoneHCID 7288—
Reactant3-(Benzyloxy)-1,2-propanediolHCID 98072—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTetrahydrofuranHCID 8028—
Product4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolaneHCID 5979252767.1%

Reaction Steps

To a tetrahydrofuran (30 ml) solution of DL-α-O-benzyl glycerol (3 g, 16.5 mmol), 3-pentanone (17.5 ml, 165 mmol) and p-toluenesulfonic acid monohydrate (300 mg, 1.58 mmol) were added at room temperature and the mixture was stirred at the same temperature for 22 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (5 ml) was added to adjust pH to about 8. The generated precipitate was removed by filtration and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient). A desired fraction was concentrated to obtain the title compound (2.77 g, 67.1% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425634B2
Source datasetuspto-grants-2008_09
ORD IDord-b0ba235f52084fb9baa50225f74f6979
Source noteuspto-grants-2008_09