HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359357Generated: November 1, 2026
Ethylene Glycol → 1,4,8-Trioxaspiro[4.5]decane
https://huagongshe.com/reaction/2359357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Tetrahydropyran | HCID 8894 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1,4,8-Trioxaspiro[4.5]decane | HCID 53440519 | 90.1% |
Reaction Steps
Tetrahydro-4H-pyran (6.00 g, 60.0 mmol) was dissolved in benzene (120 mL), to which ethylene glycol (11.2 g, 180 mmol) and p-toluenesulfonic acid monohydrate (1.14 g, 6.00 mmol) were added. Using a Dean-Stark tube, the resulting mixture was refluxed for two hours while removing water generated. To the resulting reaction liquid, a saturated aqueous solution of sodium bicarbonate was added, followed by extraction with ethyl acetate. The resulting organic layer was washed with saturated brine, and dried over sodium sulfate. The solvent was distilled off under reduced pressure. The residue thus obtained was purified by basic silica gel column chromatography (hexane:ethyl acetate, 100:0-0:100, V/V) to give the desired title compound (7.79 g, yield 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685981B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8b80f94449e743d9a586de6d7cfe7135 |
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| Source note | uspto-grants-2014_04 |
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