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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637152Generated: October 25, 2026

Dimethadione → 2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisole

https://huagongshe.com/reaction/1637152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethadioneHCID 3081—
ReactantPotassium CarbonateHCID 11430—
Reactant2-[3-(1-Adamantyl)-2-chloro-3-oxopropanamido]-4-nitroanisoleHCID 19347758—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisoleHCID 5387966679.8%

Reaction Steps

A suspension of 16.28 g (0.04 mol) of [4], 5.17 g (0.04 mol) of 5,5-dimethyloxazolidine-2,4-dione, and 16.58 g (0.12) mol of anhydrous potassium carbonate in 380 mL of dried acetone was refluxed for 3 hours. Thin layer chromatographic analysis indicated that the reaction was complete. The reaction mixture was concentrated in vacuo to yield an orange-colored solid. It was dissolved in ethyl acetate and the organic layer was washed with HCl (10%) and brine until neutrality. The organic layer was dried, filtered, and concentrated to yield an oil which solidified upon standing. It was triturated in ligroin. The final dried product (15.92 g, 79.8%) gave one spot on TLC. All analytical data confirmed the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040126
Source datasetuspto-grants-2000_03
ORD IDord-8147e9c6089444d39b250676fc062f57
Source noteuspto-grants-2000_03