摘要:
3,4-DICYANO-1.2,5-THIADIAZOLE AND 3,4 - DICHLORO - 1,2,5THIADIAZOLE ARE PREPARED FROM HYDROGEN CYANIDE, A TERTIARY AMINE, CHLORINE, AND SULFUR OR SULFUR DICHLORIDE.
摘要:
Cyclization of a dialkali metal salt of 1,1,2,3-4,4-hexacyano-2butenediide with acid yeilds 1-amino-2,3-4,5,5pentacyanocyclopentadiene which is converted to 1-amino-2,34,5,5-tetracyanocyclopentadiene which is converted to 1-amino2,3,4,5-tetracyanocyclopentadiene with strong mineral acid. Reaction of the pentacyanocyclopentadiene with nitrous acid gives 1-diaza-2,3,4,5-tetracyanocyclopentadiene which can be reacted with trialkyl or triaryl phosphorus to give 1-tri(aryl or alkyl)phosphazino-2,3,4,5-tetracyanocyclopentadiene. The diazotetracyanocyclopentadiene compound can be reacted with alkali metal compounds preferably under reducing condition to yield salts wherein the diazo group is replaced with hydrogen, amino, cyano, hydroxy, carboxy, alkoxycarbonyl, alkyl, aryl, phydroxyphenyl, nitro and mercapto groups. The cyanocyclopentadiene compounds are useful as rodenticides and as rocket propellants.
摘要:
PYROLYSIS OF 2-DIAZO-4,5-DICYANO-2H-IMIDAZOLE IN THE PRESENCE OF CERTAIN HALOHYDROCARBONS YIELDS 1 SUBSTITUTED-2-HALO-4,5-DICYANOIMIDAZOLES. -HYDROCARBON PYR LYSUS OF THE SAME STARTING MATERIAL IN THE PRESENCE OF HYDROCARBONS, CERTAIN OTHER HALOHYDROCARBONS, OR CERTAIN GROUP I METAL SALTS, YIELDS 2-SUBSTITUTED-4,5-DICYANOIMIDAZOLES.
摘要:
CYANOGEN CHLORIDE REACTS WITH DIAMINOMALENITRILE AT ABOUT AMBIENT TEMPERATURE TO PRODUCE 2-AMINO-4,5-DICYANOIMIDAZOLE. REACTION OF THE PRODUCT WITH ACID AND AN ALKALI METAL NITRITE GIVES 2-DIAZO-4,5-DICYANO-2H-IMIDAZOLE, WHICH IS USEFUL AS AN EXPLOSIVE. THE 2-AMINO-4,5DICYANOIMIDAZOLE IS USEFUL AS A CHEMICAL INTERMEDIATE AND AS A BUFFERING AGENT.