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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1637152생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1637152

반응식

참여 물질

역할이름HCID투입량
반응물DimethadioneHCID 3081—
반응물Potassium CarbonateHCID 11430—
반응물2-[3-(1-Adamantyl)-2-chloro-3-oxopropanamido]-4-nitroanisoleHCID 19347758—
용매AcetoneHCID 180—
용매Ethyl AcetateHCID 8857—
생성물2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisoleHCID 5387966679.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06040126
출처 데이터셋uspto-grants-2000_03
ORD IDord-8147e9c6089444d39b250676fc062f57
출처 메모uspto-grants-2000_03