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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Ethyl-2-hydroxybenzaldehyde | HCID 10236017 | — |
| Reactant | 4-Methylsulfonyloxymethyl-1,3-dioxane | HCID 18941616 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Ethyl-2-(1,3-dioxan-4-ylmethoxy)benzaldehyde | HCID 18941614 | 55.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0001759 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-78ee1c41d0214d01899771ef4a24d8d5 |
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| Source note | uspto-grants-1998_11 |
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