Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355272Generated: October 27, 2026

Water → 4-Ethyl-2-(1,3-dioxan-4-ylmethoxy)benzaldehyde

https://huagongshe.com/reaction/355272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Ethyl-2-hydroxybenzaldehydeHCID 10236017—
Reactant4-Methylsulfonyloxymethyl-1,3-dioxaneHCID 18941616—
SolventDimethylformamideHCID 6228—
Product4-Ethyl-2-(1,3-dioxan-4-ylmethoxy)benzaldehydeHCID 1894161455.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred solution of 3.8 grams (0.026 mole) of 5-ethyl-2-formylphenol, 5.0 grams (0.026 mole) of 4-methylsulfonyloxymethyl-1,3-dioxane, and 7.0 grams (0.051 mole) of potassium carbonate in 150 mL of N,N-dimethylformamide was heated at 80° C. for about 18 hours. Analysis by thin layer chromatography (TLC) indicated the reaction was not complete. An additional 2.5 grams (0.013 mole) of 4-methylsulfonyloxymethyl-1,3-dioxane was added, and the reaction mixture was heated at 80° C. for an additional five hours. After this time the reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with aqueous 10% lithium chloride, dried with magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was purified by column chromatography on silica gel, yielding 3.6 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0001759
Source datasetuspto-grants-1998_11
ORD IDord-78ee1c41d0214d01899771ef4a24d8d5
Source noteuspto-grants-1998_11