HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926565Generated: October 30, 2026
2,2-Dimethyl-1,3-dioxane-4,6-dione → 5-(4-(1H-1,2,4-triazol-1-yl)benzyl)-2,2-dimethyl-1,3-dioxane-4,6-dione
https://huagongshe.com/reaction/926565
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | Hantzsch ester | HCID 70849 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 4-(1H-1,2,4-triazol-1-yl)benzaldehyde | HCID 2776488 | — |
| Reactant | 2-(4-(1H-1,2,4-triazol-1-yl)benzyl)malonic acid | HCID 86715625 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-(4-(1H-1,2,4-triazol-1-yl)benzyl)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 86715624 | — |
Reaction Steps
L-Proline (1.81 g, 15.6 mmol) was added to a stirring, heterogeneous mixture of 4-(1H-1,2,4-triazol-1-yl)benzaldehyde (13.5 g, 78.0 mmol, Intermediate 82: step a) and 2,2-dimethyl-1,3-dioxane-4,6-dione (11.2 g, 78.0 mmol) in ethanol (520 mL) at 23° C. After 1.5 hours, diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate (19.7 g, 78.0 mmol) was added in one portion. After 16 hours, the ethanol was removed by rotary evaporation at 35° C. to afford a yellow solid. Isopropanol (300 mL) was added and the heterogeneous mixture was stirred for 10 minutes at 23° C. The mixture was filtered and the filter cake was washed with isopropanol (150 mL). The solids were collected and dried under vacuum to provide the titled compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284308B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-c41f05ce4cf746899a384443f25e3e3a |
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| Source note | uspto-grants-2016_03 |
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