Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173653Generated: November 1, 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → HCID 59556864, compound

https://huagongshe.com/reaction/1173653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 67105637HCID 67105637—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59556864HCID 5955686411%

Reaction Steps

To a solution of N-(3-chloro-4-cyanophenyl)valine (5.66 g), Meldrum's acid (3.39 g) and 4-(N,N-dimethylamino)pyridine (4.11 g) in tetrahydrofuran (70 mL) was added N,N′-carbonyldiimidazole (4.36 g) at 0° C., and the mixture was stirred at room temperature overnight. A 5% aqueous potassium hydrogen sulfate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with 5% aqueous potassium hydrogen sulfate solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (70 mL), and the mixture was refluxed for 45 min. After allowing to room temperature, the organic layer was washed with water and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was washed with ethyl acetate-isopropyl ether to give the title compound as colorless crystals (yield: 653 mg, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834051B2
Source datasetuspto-grants-2010_11
ORD IDord-3ebe9bcbd40b452ea4d93abb5715eb1e
Source noteuspto-grants-2010_11