Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

5-methyl-2,4-dinitroanisole synthesis

15synthesis methods
-

Yield:3606-21-1 95%

Reaction Conditions:

with potassium hydroxide at 20 - 30; for 0.5 h;

Steps:

2D Example 2D

To a suspension of l-fluoro-5-methyl-2,4-dinitro-benzene (100 g, 0.5 mol) in methanol (0.5 L) was added KOH (56 g, 0.1 mmol) in methanol (0.5 mL) drop wise at 25-30 °C. Then the resulting suspension was stirred at room temperature over a period of 30 minutes. The reaction mixture was quenched with water at 0-5 °C, the reaction mixture was filtered and dried under vacuum to obtain l-methoxy-5-methyl-2,4-dinitro-benzene as off-white solid (101 g, 95%).1H NMR (DMSO-d6, 300 MHz): 2.67 (s, 3H), 4.05 (s, 3H), 7.52 (s, 1H), 8.65 (s, 1H);LC-MS (ESI): 211.0 (M-H)

References:

WO2014/195896,2014,A1 Location in patent:Page/Page column 34-36

5-methyl-2,4-dinitroanisole Related Search: