Literature DB >> 16092836

A new practical one-pot conversion of phenols to anilines.

Masahiro Mizuno1, Mitsuhisa Yamano.   

Abstract

A novel one-pot synthesis of anilines from phenols was developed. Using this methodology, anilines are produced in good yield (86%) by a reaction of phenols with 2-bromo-2-methylpropionamide and NaOH in DMA via Smiles rearrangement. Phenols, which are substituted electron-withdrawing groups, are more reactive for Smiles rearrangement. Thiophenols are also converted to anilines. The process is a convenient, safe, and inexpensive method for large-scale preparation of anilines. [reaction: see text]

Entities:  

Year:  2005        PMID: 16092836     DOI: 10.1021/ol051080k

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

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Authors:  Matthew D Hammers; Loveprit Singh; Leticia A Montoya; Alan D Moghaddam; Michael D Pluth
Journal:  Synlett       Date:  2016       Impact factor: 2.454

2.  Enantiospecific synthesis of genetically encodable fluorescent unnatural amino acid L-3-(6-acetylnaphthalen-2-ylamino)-2-aminopropanoic acid.

Authors:  Zheng Xiang; Lei Wang
Journal:  J Org Chem       Date:  2011-07-06       Impact factor: 4.354

3.  Discovery of Potent and Selective Agonists of δ Opioid Receptor by Revisiting the "Message-Address" Concept.

Authors:  Qing Shen; Yuanyuan Qian; Xiaoqin Huang; Xuejun Xu; Wei Li; Jinggen Liu; Wei Fu
Journal:  ACS Med Chem Lett       Date:  2016-02-10       Impact factor: 4.345

4.  Synthesis of 7-Aminocoumarins from 7-Hydroxycoumarins via Amide Smiles Rearrangement.

Authors:  Daniel S Lippe; Omar Elghawy; Adam M Zucker; Evan S K Yanagawa; Erin Mathews; Yusef G Ahmed; Paige N D'Elia; Sabrina Bimson; Ryan R Walvoord
Journal:  ACS Omega       Date:  2022-09-21
  4 in total

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