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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantHantzsch esterHCID 70849—
ReactantL-ProlineHCID 145742—
Reactant4-(1H-1,2,4-triazol-1-yl)benzaldehydeHCID 2776488—
Reactant2-(4-(1H-1,2,4-triazol-1-yl)benzyl)malonic acidHCID 86715625—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Product5-(4-(1H-1,2,4-triazol-1-yl)benzyl)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 86715624—

Reaction Conditions

Temperature23 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-c41f05ce4cf746899a384443f25e3e3a
Source noteuspto-grants-2016_03