Sulphuric acid immobilized on silica gel (H2SO4–SiO2) as an eco-friendly catalyst for transamidation

RSC Advances ◽  
2015 ◽  
Vol 5 (14) ◽  
pp. 10567-10574 ◽  
Author(s):  
Sk. Rasheed ◽  
D. Nageswar Rao ◽  
A. Siva Reddy ◽  
Ravi Shankar ◽  
Parthasarathi Das

A novel method of transamidation of carboxamides with amines using catalytic amounts of H2SO4–SiO2 under solvent-free conditions has been developed. The scope of the methodology has been demonstrated with primary and secondary amines.

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Davood Habibi ◽  
Payam Rahmani ◽  
Ziba Akbaripanah

N-formylation of primary and secondary amines was carried out with formic acid in the presence of silica sulfuric acid under solvent-free conditions to give the corresponding formamides in excellent yield and short reaction times.


2019 ◽  
Vol 48 (10) ◽  
pp. 3447-3452 ◽  
Author(s):  
Alexandra A. Ageshina ◽  
Grigorii K. Sterligov ◽  
Sergey A. Rzhevskiy ◽  
Maxim A. Topchiy ◽  
Gleb A. Chesnokov ◽  
...  

A single catalyst for solvent-free Buchwald–Hartwig amination with both primary and secondary amines.


2014 ◽  
Vol 68 (3) ◽  
Author(s):  
Davood Habibi ◽  
Payam Rahmani ◽  
Ziba Akbaripanah

AbstractThe thioacetalisation of a variety of heterocyclic, aromatic, and aliphatic carbonyl compounds (1 mmol) with ethane-1,2-dithiol (1 mmol) using silica sulphuric acid (SSA) is presented as an efficient heterogeneous catalyst under mild and solvent-free conditions at 60°C. The thioacetals were formed within a short reaction time (1–34 min) and isolated with 90–98 % yield following an extractive procedure and chromatography on silica gel. The competitive protection reaction between aldehyde and ketone with ethane-1,2-dithiol afforded the protected derivatives of benzaldehyde and acetophenone with 92 % and 8 % yields, respectively, indicating some selectivity.


1999 ◽  
Vol 23 (2) ◽  
pp. 128-129
Author(s):  
Mohammad M. Mojtahedi ◽  
Mohammad R. Saidi ◽  
Mohammad Bolourtchian

The reaction of primary and secondary amines with epoxides in the presence of montmorillonite K10 clay, under solvent-free condtions and microwave irradiation affords high yields of β-amino alcohols.


1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.


2021 ◽  
pp. 1-10
Author(s):  
Gholamhassan Imanzadeh ◽  
Havva Rezaei ◽  
Roghayyeh Asgharzadeh ◽  
Zahra Soltanzadeh

2015 ◽  
Vol 17 (5) ◽  
pp. 3157-3163 ◽  
Author(s):  
Andrea Ojeda-Porras ◽  
Alejandra Hernández-Santana ◽  
Diego Gamba-Sánchez

A highly improved methodology for the direct amidation of carboxylic acids with amines using silica gel as a solid support and catalyst is described. Several examples using aliphatic, aromatic, unsaturated and fatty acids combined with primary and secondary amines are shown.


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