HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494426Generated: October 31, 2026
1,4-Dioxane → 5-Hydroxy-4-([3,4-methylenedioxyphenyl]methyl)-2(5H)-furanone
https://huagongshe.com/reaction/1494426
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,3-Benzodioxole-5-propanal | HCID 169203 | — |
| Reactant | Piperidine, hydrochloride (1:1) | HCID 2723721 | — |
| Reactant | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Hydroxy-4-([3,4-methylenedioxyphenyl]methyl)-2(5H)-furanone | HCID 14750909 | 28.5% |
Reaction Steps
2.5 g (0.027 mol) of glyoxylic acid hydrate, 3.2 g (0.027 mol) of piperidine hydrochloride, and 30 mL of dioxane were mixed with stirring, whereupon water was added in dropwise fashion until a homogeneous solution resulted. 3-(3,4-Methylenedioxyphenyl)propionaldehyde (4.8 g, 0.027 mol) was then introduced and the solution allowed to stir at room temperature for 1 hour, then heated at reflux for 48 hours. At the end of this time the solution was concentrated, diluted with water, and extracted with EtOAc (2×100 mL). The organic layer was separated, dried (MgSO4) then concentrated to afford an oil. The crude oil was chromatographed over silica gel (150 g). Elution with 50% EtOAc-hexane afforded 1.8 g, 28% of the desired product as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026725 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-0f46d3482e0346c89a02d41db77629c2 |
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| Source note | uspto-grants-1991_06 |
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