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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345029생성일: 2026년 10월 25일

Sodium Iodide → N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamine

https://huagongshe.com/reaction/345029

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물2-(Chloromethyl)-5-nitro-1,3-benzoxazoleHCID 2764189—
반응물N-methyl-4-nitrophenethylamineHCID 2794239—
용매AcetonitrileHCID 6342—
생성물N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamineHCID 19813428—

반응 단계

2-Chloromethyl-5-nitrobenzoxazole (2.85 g, 13.4 mmole), N-methyl-4-nitrophenethylamine (J.O.C., [1956], 21, 45) (2.2 g, 12.2 mmole), potassium carbonate (1.85 g, 13.4 mmole) and sodium iodide (2.0 g, 13.4 mmole) were heated under reflux in acetonitrile (50 ml) for 3 days. The solvent was then evaporated, the residue diluted with water, and extracted three times with methylene chloride. The combined organic extracts were washed with water, dried (MgSO4), filtered and evaporated to dryness. The resultant oil was diluted with ether and the supernatant decanted and evaporated to dryness to give an orange solid, which was recrystallised from isopropanol to give the title compound, yield 0.80 g. 'H-N.m.r. (CDC13): δ=8.6 (d, 1H); 8.3 (dd, 1H); 8.1 (d, 2H); 7.6 (d, 1H); 7.35 (d, 2H); 3.95 (s, 2H); 2.95 (q, 2H); 2.85 (q, 2H); 2.5 (s, 3H) p.p.m.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05055473
출처 데이터셋uspto-grants-1991_10
ORD IDord-16a4d8d778994655bd85a543ff7226e3
출처 메모uspto-grants-1991_10