Some p-Nitrophenyl Derivatives of o-Phosphoric and o-thiophosphoric Acid

1950 ◽  
Vol 72 (12) ◽  
pp. 5777-5777 ◽  
Author(s):  
J. A. A. Ketelaar ◽  
H. R. Gersmann
1989 ◽  
Vol 44 (12) ◽  
pp. 1545-1549 ◽  
Author(s):  
Konrad Giersdorf ◽  
Ursula Diefenbach ◽  
Udo Engelhardt

(Cl—CH2CH2)2N—P(=X)Cl2, X = O, reacts with 1,2-dimethylhydrazine in the presence of triethylamine to give the dihydrazide. Hexahydropyridazine as “cyclic hydrazine” leads to a tetracyclic side product formed by HCl elimination from the reactive 2-chloroethyl groups and active β-NH protons of the hexahydropyridazinyl substituents. The corresponding thio-compound, X = S. yields the monosubstitution product (Cl—CH2CH2)2N—P(=S)(N(CH3)—N(CH3)H)Cl. O-Benzylhydroxyamine hydrochloride substitutes both Cl-atoms at P to ioni (Cl—CH2CH2)2N—P(=S)(NH—O—CH2—C6H5)2. The corresponding phenylesters C6H5O—P(=X)(NH—O–CH2—C6H5)2, X = O, S, are prepared in a similar reaction.


2004 ◽  
Vol 14 (13) ◽  
pp. 3473-3476 ◽  
Author(s):  
Webster L. Santos ◽  
Brian H. Heasley ◽  
Renata Jarosz ◽  
Karen M. Carter ◽  
Kevin R. Lynch ◽  
...  

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