Diacetylmelamine and
o-(or
m- or
p-) nitrobenzoic anhydride (NBA) in the molar ratio of 1: 2 are reacted by fusion at around 200°C to obtain mono-
o-onitrobenzoyl-diacetylmelamine (1) or corresponding
m-isomer (2) and
p-isomer (3). A partial saponification of (1), (2), and (3) with 5% aqueous solution of sodium hydroxide yielded mono-
o-nitrobenzoylmelamine (4), and corresponding
m-(5) and
p-isomer (6), respectively. These mono-substituted products are also obtainable by boiling melamine (M) in dioxane and
o-(or
m- or
p-) NBA in the molar ratio of 1: 2. Reaction of (4) and
o-NBA, (5) and
m-NBA, and (6) and
p-NBA in dioxane yielded di-
o-nitrobenzoylmelamine (7), and corresponding
m-iosmer (8), and
p-isomer (9). Reaction by fusion of M and
o-NBA at around 160°C M and
m- and
p-NBA at around 200°C in their molar ratio of 1: 4.5 yielded tri-
o-nitrobenzoylmelamine 10), and corresponding misomer 11), and
p-isomer (12). The products (1)-(12) are new compounds.
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