| Full text | |
| Author(s): |
Santos Nascimento, Lillian Ferreira
;
Santos Fernandes, Joao Paulo
Total Authors: 2
|
| Document type: | Journal article |
| Source: | GREEN PROCESSING AND SYNTHESIS; v. 6, n. 2, p. 203-209, APR 2017. |
| Web of Science Citations: | 0 |
| Abstract | |
N-allylanilines are important compounds that are used to access several bioactive compounds containing indole and dihydroindole nucleus. However, their preparation through allylation can lead to the undesirable N, N-diallyl byproduct. In this work, the N-allylation of 4-chloroaniline was studied. In order to accelerate the process and maximize the monoallylated: diallylated ratio, we reported two full factorial studies to transpose the conventional synthetic procedure to an ultrasound (US) methodology. The evaluated factors were temperature, quantity of reagents (allyl bromide and K2CO3), reaction time, and methodology (conventional or US). The results showed that US did not change the monoallylated: diallylated ratio, but significantly improved the reaction rate, giving increased average monoallylated and total yields of 11.4% and 18.1%, respectively (p < 0.05). The proposed US methodology gave the same yields and product ratio in a 4-h reaction time than the conventional 24-h procedure, without heating and using only an inexpensive US bath to conduct the reactions. (AU) | |
| FAPESP's process: | 13/20479-9 - Synthesis and evaluation of compounds potentially ligands of H4 receptors |
| Grantee: | João Paulo dos Santos Fernandes |
| Support Opportunities: | Regular Research Grants |