摘要:
Novel polysubstituted 2-keto-1,4- diazacycloalkanes are powerful stabilizers for materials subject to ultraviolet (UV) light degradation, particularly for polyolefins. The cyclic 2-keto compounds of this invention have (a) a fixed two-carbon bridge between the N'and N 4 atoms of the diaza ring, the remaining portion of the ring having a variable length bridge of two or more carbon atoms, (b) an N-adjacent carbonyl in the fixed two-carbon bridge, and (c) at least one N 4 -adjacent carbon atom of the diaza ring is polysubstituted, that is, has two substituents which may be cyclizable. Compositions containing (a) the polysubstituted 2- keto-1,4- diazacycloalkanes of this invention, and (b) prior art polysubstituted 2-keto-1,4- diazacycloalkanes, exhibit excellent stability to UV light.
摘要:
A novel synthesis has been discovered for preparation of 2-keto-1,4-diazacycloalkanes and their derivatives. Trans isomers of polysubstituted quinoxalin-2-ones may now be prepared.
摘要:
A novel synthesis has been discovered for preparation of 2-keto-1,4-diazacycloalkanes and their derivatives. Trans isomers of polysubstituted quinoxalin-2-ones may now be prepared.
摘要:
Several novel syntheses have been discovered for preparation of 2-keto-1,4- diazacycloalkanes and their derivatives. Trans isomers of polysubstituted quinoxalin-2- ones may now be prepared.
摘要:
A process is disclosed for making a 1,4-diazacycloheptan-2-one from a mixture ('first' mixture) of alkylated 1,3-propanediamines one of which (referred to as the 'target' diamine) has substituents at specifed positions and contains (i) a terminal primary amine group adjacent to a disubstituted C atom (hence, referred to as having a 'hindered' N atom), and (ii) a terminal secondary amine group. The target diamine, other diamines and oligomeric polyamines in the first mixture, are made by alkylating an acyclic ('starting') 1,3-propanediprimaryamine having the hindered N atom. The first mixture of alkylated diamines, preferably containing a major molar proportion of the target diamine relative to any other alkylated diamines, is reductively alkylated, which unexpectedly results in the reductive alkylation of only the unwanted diamines, allowing the target diamine which is not reductively alkylated, to be removed from the mixture of reductively alkylated diamines. Upon cyclization of the target diamine, using the "ketoform reaction", it is essentially quantitatively converted to the 1,4-diazacycloheptan-2-one having an unsubstituted N⁴ atom flanked by disubstituted adjacent C atoms. By removing the unwanted components in the reaction mass an essentially pure product of 1,4-diazacycloheptan-2-ones is recovered. Thus, the difficulty of separating the target amine from other close-boiling compounds is avoided. As an alternative, the reductive alkylation step can be bypassed and the first mixture subjected to the ketoform reaction, followed by recovery of the desired product.