WebBaeyer–Drewsen indigo synthesis. The Baeyer–Drewsen indigo synthesis (1882) is an organic reaction in which indigo is prepared from 2-nitrobenzaldehyde and acetone [1] [2] The reaction was developed by von Baeyer in 1880 to produce the first synthetic indigo at laboratory scale. This procedure is not used at industrial scale. WebThe Bernthsen acridine synthesis is the chemical reaction of a diarylamine heated with a carboxylic acid (or acid anhydride) and zinc chloride to form a 9-substituted acridine. [1] …

Synthesis of Acridone Derivatives Using Polymer ... - ResearchGate

WebBernthsen Acridine Synthesis Formation of 5-substituted acridines by heating diarylamines in organic acids or anhydrides, usually in the presence of zinc chloride: You are able to … WebBernthsen Synthesis. A. Bernthsen, Ann. 192, 1 (1878); 224, 1 (1884). Formation of 5-substituted acridines by heating diarylamines in organic acids or anhydrides, … sewing stocking stuffer ideas

A convenient synthesis of 2-amino-5,6,7,8,-tetrahydro-5-oxo-4 …

WebThe reaction mixture is heated at high temperature (above 200°C) for a * email: [email protected] very log time (48 h). The Bernthsen reaction requires catalysts as anhydrous zinc chloride or polyphosphoric acid, but the yield reaches only 18-20% [20, 21]. Previously, we obtained acridine derivatives by Bernthsen method [18,22]. Web3 in Bernthsen reaction (reaction of DPA and benzoic acid was chosen as the model reaction) under thermalas wellas MWI in the absence of solvent. However, the best results in terms of yields and reaction time were obtained with p-TSA (Table 1) under MWI. CAN and basic alumina also afforded the products but yields were poorer. In order to the tunneling company