돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1645484생성일: 2026년 10월 25일

N-Methylallylamine → 3-(Allyl-methyl-carbamoyl)-5-amino-2,4,6-triiodo-benzoyl chloride

https://huagongshe.com/reaction/1645484

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylallylamineHCID 69391—
반응물5-Amino-2,4,6-triiodoisophthaloyl dichlorideHCID 9894858—
용매TetrahydrofuranHCID 8028—
생성물3-(Allyl-methyl-carbamoyl)-5-amino-2,4,6-triiodo-benzoyl chlorideHCID 59824364—

반응 단계

Typically 5-amino-2,4,6,triiodoisophthaloyl dichloride (1) (100 g, 168 mmol) was dissolved in anhydrous THF (500 ml), the N-methyl allylamine (25 ml) was dissolved in 50 ml THF, and added dropwise to the solution over 1 hour. The mixture was heated to 50 deg C. and stirred overnight. The crude mixture was analysed by LCMS and this confirmed that the reaction mixture contained the desired product, ‘bis-acid chloride’ and ‘bis-N-methyl-allylamide’. The reaction was also monitored by TLC (2% MeOH in DCM) on silica gel plates, bis-acid chloride had an Rf of ˜0.98, the mono-N-methylallylamide ˜0.73 and the bis-N-methylallylamide ˜0.25. Once the reaction was deemed complete, the solution was filtered, vacuumed to dryness, then dissolved in 500 ml of ethyl acetate this solution was then loaded onto silica and purified on a 750 g column using ethyl acetate (B) and petrol (A) (10%→100% B over ˜10 column volumes). The pure fractions were collected and identified by TLC, the desired fractions were then vacuumed to dryness. The structure was confirmed by 1H and 13C NMR and purity by LCMS.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124806B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-d1dd68829aaa4b7c8093b7a841372198
출처 메모uspto-grants-2012_02