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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345514생성일: 2026년 10월 26일

tert-Butylacrylamide → N-tert-butyl-[3-(N,N-dibenzylaminoxy)-propionamide]

https://huagongshe.com/reaction/345514

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButylacrylamideHCID 7877—
반응물DibenzylhydroxylamineHCID 69297—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물N-tert-butyl-[3-(N,N-dibenzylaminoxy)-propionamide]HCID 14297377—

반응 단계

A solution of 21.33 g of dibenzylhydroxylamine in 100 ml of dry tetrahydrofuran is admixed with 1.12 g of potassium-tert-butoxide followed by 12.70 g of N-tert-butylacrylamide. The solution is heated under reflux for 24 hours under N2. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, brine dried (MgSO4) and evaporated under reduced pressure. Purification by liquid chromatography affords the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057563
출처 데이터셋uspto-grants-1991_10
ORD IDord-93ff27e0422a4cc28e2a15a9a0978d7d
출처 메모uspto-grants-1991_10