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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 546583생성일: 2026년 10월 25일

Sodium hydride → 3-(4-Tert-butylphenyl)-1-[(2-chloropyridin-4-yl)methyl]-5,5-dimethylimidazolidine-2,4-dione

https://huagongshe.com/reaction/546583

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-4-(chloromethyl)pyridineHCID 11126573—
반응물3-(4-Tert-butylphenyl)-5,5-dimethyl-imidazolidine-2,4-dioneHCID 57625972—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-(4-Tert-butylphenyl)-1-[(2-chloropyridin-4-yl)methyl]-5,5-dimethylimidazolidine-2,4-dioneHCID 5762597163.5%

반응 단계

To a suspension of 1.1 g of sodium hydride in 40 mL of dimethylformamide under argon are successively added 4.9 g of 3-(4-tert-butylphenyl)-5,5-dimethylimidazolidine-2,4-dione obtained in stage c) of Example 1 and 4.55 g of 2-chloro-4-(chloromethyl)pyridine. The reaction mixture is stirred for 48 hours at room temperature and then diluted with 260 mL of water. The solid formed is filtered off, rinsed with diisopropyl ether and dried to give 4.61 g of 3-(4-tert-butylphenyl)-1-[(2-chloropyridin-4-yl)methyl]-5,5-dimethylimidazolidine-2,4-dione in the form of a beige-coloured powder, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935819B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-7c53bd76a9bd4d68940eca962bf2a48f
출처 메모uspto-grants-2011_05