Synthesis of 2-methyl-4-selenoquinazolone, 2-phenylbenzoselenazole, and its derivatives / Dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Faculty of Pure Science of Columbia University

by Yü-Gwan Chen

Monobenzylidene Derivative

Five grams of the monoamino compound were dissolved in 200 cc. absolute alcohol with the addition of 3 cc. of benzaldehyde and the clear solution was boiled on a water-bath, with a return condenser, for two hours. After the solution was boneblacked, the yellow precipitate was recrystallized from carbon disulphide. The yield was 90 per cent.

It crystallizes in yellow plates, melting at 156.7°-157.6°C., soluble in benzene, ether, ethyl alcohol, carbontetrachloride, acetone, but difficultly soluble in ligroin. An analysis of the crystals showed the following result,

	Calculated for C20H14N2Se	Found
Nitrogen	7.75%	7.92%	7.68%