Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

291536-35-1

(Z)-5-(4-Fluorobenzylidene)thiazolidine-2,4-dione synthesis

2synthesis methods
2295-31-0 Synthesis
2,4-Thiazolidinedione

2295-31-0
511 suppliers
$6.00/5g

(Z)-5-(4-Fluorobenzylidene)thiazolidine-2,4-dione

291536-35-1
9 suppliers
inquiry

-

Yield:291536-35-1 97%

Reaction Conditions:

with Fe3O4/SiO2-NH2/Cu(II) in ethanol; for 0.5 h;Catalytic behavior;Reflux;Green chemistry;

Steps:



General procedure: To a mixture of thiazolidine-2,4-dione or rhodanine(0.13 g, 1 mmol), aliphatic/aromatic aldehyde (1 mmol), and ethanol (4 ml), a portion of Fe3O4/SiO2-NH2/Cu(II) (0.15 g) was added and the mixture stirred under reflux for the required time (Table 2). The progress of the reaction was monitored by TLC (n-hexane/EtOAc, 2:1). After completion of the reaction, EtOH (3 ml) was added and the nanocatalyst was separated by an external magnet. The crude product was recrystallized from EtOH.

References:

Akhavan, Malihe;Foroughifar, Naser;Pasdar, Hoda;Khajeh-Amiri, Alireza;Bekhradnia, Ahmadreza [Transition Metal Chemistry,2017,vol. 42,# 6,p. 543 - 552]