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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 67105637 | HCID 67105637 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59556864 | HCID 59556864 | 11% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834051B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-3ebe9bcbd40b452ea4d93abb5715eb1e |
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| Source note | uspto-grants-2010_11 |
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