Unknown

Dataset Information

0

Phosphonium acidic ionic liquid: an efficient and recyclable homogeneous catalyst for the synthesis of 2-arylbenzoxazoles, 2-arylbenzimidazoles, and 2-arylbenzothiazoles.


ABSTRACT: A highly efficient and green strategy for the synthesis of 2-arylbenzoxazoles, 2-arylbenzimidazoles, and 2-arylbenzothiazoles catalyzed by phosphonium acidic ionic liquid has been developed via the condensation of o-aminophenol, o-phenylenediamines, and o-aminothiophenol, respectively, with aldehydes. The reaction has a good yield, the broad substrate scope, and mild condition. Triphenyl(butyl-3-sulphonyl)phosphonium toluenesulfonate catalyst was easily obtained from cheap and available starting materials through a one-pot synthesis. Its structure was identified by 1H NMR, 13C NMR, 31P NMR, and FT-IR techniques. Other properties including thermal stability and acidity were determined by TGA and Hammett acidity function method. Interestingly, the catalyst can maintain its constantly outstanding performance till the fourth recovery.

SUBMITTER: Nguyen QT 

PROVIDER: S-EPMC9079114 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Phosphonium acidic ionic liquid: an efficient and recyclable homogeneous catalyst for the synthesis of 2-arylbenzoxazoles, 2-arylbenzimidazoles, and 2-arylbenzothiazoles.

Nguyen Quang The QT   Thi Hang Anh-Hung AH   Ho Nguyen Thuy-Linh TL   Nguyen Chau Duy-Khiem DK   Tran Phuong Hoang PH  

RSC advances 20180327 21


A highly efficient and green strategy for the synthesis of 2-arylbenzoxazoles, 2-arylbenzimidazoles, and 2-arylbenzothiazoles catalyzed by phosphonium acidic ionic liquid has been developed <i>via</i> the condensation of <i>o</i>-aminophenol, <i>o</i>-phenylenediamines, and <i>o</i>-aminothiophenol, respectively, with aldehydes. The reaction has a good yield, the broad substrate scope, and mild condition. Triphenyl(butyl-3-sulphonyl)phosphonium toluenesulfonate catalyst was easily obtained from  ...[more]

Similar Datasets

| S-EPMC9078748 | biostudies-literature
| S-EPMC6648500 | biostudies-literature
| S-EPMC9835634 | biostudies-literature
| S-EPMC9724129 | biostudies-literature
| S-EPMC10068824 | biostudies-literature
| S-EPMC9329924 | biostudies-literature
| S-EPMC10099423 | biostudies-literature
| S-EPMC7469116 | biostudies-literature
| S-EPMC11552662 | biostudies-literature
| S-EPMC7082613 | biostudies-literature