戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 601012作成日:2026年10月25日

Methyl iodide → 1,2,4-Trimethoxy-5-nitrobenzene

https://huagongshe.com/reaction/601012

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物4,5-Dimethoxy-2-nitrophenolHCID 297121—
溶媒DimethylformamideHCID 6228—
生成物1,2,4-Trimethoxy-5-nitrobenzeneHCID 82241557%

反応条件

温度77.5 °C

反応手順

A mixture of 4,5-dimethoxy-2-nitro-phenol (2.00 g, 10 mmol), potassium carbonate (2.76 g, 20 mmol) and iodomethane (0.75 mL, 12 mmol) in DMF was placed in a sealed tube and heated at 75-80° C. for 20 h. The reaction was cooled and was filtered through Celite, washing with ethyl acetate. The filtrate was washed with water (the first wash was back-extracted with ethyl acetate), sodium bicarbonate and brine, was dried (sodium sulfate) and was evaporated. Purification by flash chromatography (SiO2) eluted with 1:1 ethyl acetate:hexanes provided 1,2,4-trimethoxy-5-nitro-benzene (1.20 g, 57% yield) as a yellow solid. 1H-NMR (CDCl3, 500 MHz) 7.53 (s, 1H), 6.50 (s, 1H), 3.92 (s, 3H), 3.91 (s, 3H), 3.84 (s, 3H) ppm; MS (FIA) 214.1 (M+H); HPLC (Method A) 3.253 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902239B2
出典データセットuspto-grants-2011_03
ORD IDord-d0cb3f73ea544a2e9dd67cb12c01bfa6
出典メモuspto-grants-2011_03