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HRID 1637152作成日:2026年10月26日

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

https://huagongshe.com/reaction/1637152

反応式

関与物質

役割名称HCID仕込み量
反応物DimethadioneHCID 3081—
反応物Potassium CarbonateHCID 11430—
反応物2-[3-(1-Adamantyl)-2-chloro-3-oxopropanamido]-4-nitroanisoleHCID 19347758—
溶媒AcetoneHCID 180—
溶媒Ethyl AcetateHCID 8857—
生成物2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisoleHCID 5387966679.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06040126
出典データセットuspto-grants-2000_03
ORD IDord-8147e9c6089444d39b250676fc062f57
出典メモuspto-grants-2000_03