Syntheses of di-Schiff’s bases: A comparative study using benzene and water (concept of green chemistry) as solvents | Zendy

Gita Chawla | Zendy; Muhamad Thufail | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

Syntheses of di-Schiff’s bases: A comparative study using benzene and water (concept of green chemistry) as solvents

Author(s) -

Gita Chawla,

Muhamad Thufail

Publication year - 2020

Publication title -

international journal of pharmaceutical chemistry and analysis

Language(s) - English

Resource type - Journals

eISSN - 2394-2797

pISSN - 2394-2789

DOI - 10.18231/j.ijpca.2020.007

Subject(s) - schiff base , aldehyde , benzene , chemistry , catalysis , solvent , green chemistry , organic chemistry , diamine , polymer chemistry , reaction mechanism

Di-Schiff’s bases are normally synthesized from aldehyde and diamine using organic solvents under conditions that remove water azeotropically. Here is a report for the preparation of di-Schiff’s base using both the conventional method and pure water without a catalyst and results were compared. It was observed that yields are better and reaction time is comparatively less when water is used as a solvent.Keywords: Benzene, Water, Green chemistry.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research