Iron-catalyzed ortho trifluoromethylation of anilines via picolinamide assisted photoinduced C-H functionalization.
Org Biomol Chem
; 16(13): 2214-2218, 2018 03 28.
Article
em En
| MEDLINE
| ID: mdl-29528082
ABSTRACT
A convenient, oxidant-free protocol was developed for the ortho trifluoromethylation of aniline via picolinamide assisted Fe-promoted C-H functionalization under ultraviolet irradiation. In this transformation acetone essentially acted as both a solvent to dissolve reactants and a low-cost radical initiator to efficiently generate a CF3 radical from Langlois' reagent. A broad substrate scope was tolerated and picolinamide bearing strong electron withdrawing groups also could be transformed into the corresponding products with acceptable yields. Furthermore, the value of this method has been highlighted via the efficient synthesis of the nonsteroidal anti-inflammatory drug floctafenine.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Ácidos Picolínicos
/
Ferro
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Compostos de Anilina
Idioma:
En
Ano de publicação:
2018
Tipo de documento:
Article