HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684267Generated: October 27, 2026
Ethylene Glycol → Methyl 1,4-dioxaspiro[4.5]decane-7-carboxylate
https://huagongshe.com/reaction/1684267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Methyl 3-oxocyclohexane-1-carboxylate | HCID 566099 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | Methyl 1,4-dioxaspiro[4.5]decane-7-carboxylate | HCID 372311 | — |
Reaction Steps
A solution composed of 30 g (192 mmol) of crude methyl 3-oxocyclohexanecarboxylate and 430 cm3 of toluene is introduced into a one-liter three-necked flask equipped with a Dean and Stark apparatus, and 14.3 g (230 mmol) of ethylene glycol are then added with 814 mg (4.3 mmol) of para-toluenesulfonic acid monohydrate. The mixture is heated to reflux, the toluene-water azeotrope forms instantaneously and, after 40 min, no further refluxing of azeotrope (95° C.) takes place. The mixture is maintained for 6 h under reflux of the toluene (110° C.). After cooling, sodium hydrogen carbonate solution is added and the solution is then washed with saturated sodium chloride solution and dried over sodium sulfate. After concentration, 39 g of a yellow oil are obtained, which product is either distilled or chromatographed on a column of 215 g of silica (eluant: cyclo-hexane/ether, 98:2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05639902 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-33d9c668b6f747bc98779db9235d35f4 |
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| Source note | uspto-grants-1997_06 |
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