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4-AMINO-3,5-DINITROBENZOIC ACID synthesis

11synthesis methods
-

Yield:7221-27-4 98%

Reaction Conditions:

with ammonium hydroxide in methanol at 20; for 19.5 h;Reflux;

Steps:

5.1.2. 4-Amino-3,5-Dinitrobenzoic Acid (3)

Compound 2 (20 g, 81 mmol) was dissolved in methanol (100 mL), and aqueous 24% NH3 (120 mL)was gradually added. The reaction mixture was stirred at rt for 2.5 h, refluxed for 3 h and left atrt for around 14 h. The precipitate that formed was filtered o, and the filtrate was evaporated todryness. Water (10 mL) and HCl (10 mL) were added to the solid residue, which was combined withthe precipitate. After stirring for 10 min, the precipitate was filtered o and washed with water tillwashings showed neutral. The yield of 4-amino-3,5-dinitrobenzoic acid 3 was 18 g (98%) [16]. 1H NMR(300 MHz, Acetone-d6) = 9.16-9.01 (m, 3H), 9.01-8.84 (s, 2H). 13C NMR (75 MHz, Acetone-d6) 163.49, 143.33, 134.76, 133.75, 128.17, 115.39. HRMS (ESI): m/z calcd. for C7H4N3O6 [MH]: 226.0105;found, 226.0100.

References:

Aerschot, Arthur Van;Gadakh, Bharat;Lescrinier, Eveline;Nautiyal, Manesh;Pang, Luping;Rozenski, Jef;Strelkov, Sergei V.;Weeks, Stephen D.;Zhang, Baole;de Graef, Steff [Molecules,2020,vol. 25,# 20,art. no. 4751]

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