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Hydrazinecarbothioamide, 2-[(4-oxo-4H-1-benzopyran-3-yl)methylene]- synthesis

2synthesis methods
-

Yield:146618-32-8 86%

Reaction Conditions:

in ethanol; for 2 h;Reflux;

Steps:

2 2.1.1 General procedure for the synthesis of the ligands (HL1-HL4)

General procedure: Synthesis of the ligands was carried out as per the literature methods [16,17] with slight modifications. 4-oxo-4H-chromene-3-carbaldehyde (0.5g; 2.871mmol) was dissolved in 10cm3 of ethanol. To this, ethanolic solution of thiosemicarbazide/4(N)-methylthiosemicarbazide/4(N)-ethylthiosemicarbazide/4(N)-phenylthiosemicarbazide (2.871mmol) was added and the mixture was refluxed for 2h. A white compound precipitated was collected by filtration and washed well with cold ethanol and dried in vacuo.

References:

Kalaiarasi;Rajkumar, S. Rex Jeya;Dharani;Lynch, Vincent M.;Prabhakaran [Inorganica Chimica Acta,2018,vol. 471,p. 759 - 776]