《Etherification of phenols by amines via transient diazonium intermediates》 was written by Reynard, Guillaume; Mayrand, Hugo; Lebel, Helene. Reference of 3-Aminopropan-1-ol And the article was included in Canadian Journal of Chemistry in 2020. The article conveys some information:
The synthesis of alkyl aryl ethers from electron poor phenols and amines using 1,3-propanedinitrite was described. Due to the mild conditions, functionalized primary, secondary and tertiary alkyl groups were successfully introduced, denoting a highly tolerant process that allowed for unprotected alcs. and acetals. The reaction was thought to proceeded through the formation of a diazonium intermediate that undergoes subsequent SN2> or SN1 reactions. The results came from multiple reactions, including the reaction of 3-Aminopropan-1-ol(cas: 156-87-6Reference of 3-Aminopropan-1-ol)
3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Reference of 3-Aminopropan-1-ol
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