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HRID 345029作成日:2026年10月27日

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

https://huagongshe.com/reaction/345029

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物2-(Chloromethyl)-5-nitro-1,3-benzoxazoleHCID 2764189—
反応物N-methyl-4-nitrophenethylamineHCID 2794239—
溶媒AcetonitrileHCID 6342—
生成物N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamineHCID 19813428—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05055473
出典データセットuspto-grants-1991_10
ORD IDord-16a4d8d778994655bd85a543ff7226e3
出典メモuspto-grants-1991_10