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The Chemistry of Powder and Explosives - Sciencemadness Dot Org

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178 AROMATIC NITRO COMPOUNDS<br />

lized from alcohol. Pure tetryl melts at about 129.4°; a good commercial<br />

sample, at about 128.5°.<br />

<strong>The</strong> nitration <strong>of</strong> aniline in the presence <strong>of</strong> a large amount <strong>of</strong><br />

strong sulfuric acid results wholly in the formation <strong>of</strong> m-nitroaniline,<br />

but the similar nitration <strong>of</strong> dimethylaniline gives principally<br />

a mixture <strong>of</strong> the ortho- <strong>and</strong> para-derivatives. Monomethylaniline<br />

st<strong>and</strong>s between aniline <strong>and</strong> dimethylaniline in<br />

respect to the orienting effect <strong>of</strong> its amino group; it yields a<br />

considerable amount <strong>of</strong> the m-nitro- compound—<strong>and</strong> dimethylaniline<br />

is preferred for the preparation <strong>of</strong> tetryl. Commercial<br />

dimethylaniline contains a certain amount <strong>of</strong> monomethylaniline,<br />

from which it is extremely difficult to free it, <strong>and</strong> this in the<br />

manufacture <strong>of</strong> tetryl is converted in part into 2,3,4,6-tetranitrophenylmethylnitramine,<br />

or m-nitrotetryl, pale yellow, almost<br />

white, crystals from benzene, m.p. 146-147.° 87<br />

CH3 3 H CH3 H CH3 NO2 CH3 CH3 NO2<br />

V V V<br />

I<br />

V<br />

I<br />

3<br />

» H20 ]<br />

J-NO2 i I<br />

H,o<br />

J-NO2 J-NO, I \ J-OH / °<br />

NO2<br />

NO,<br />

No m-nitrotetryl is produced if pure dimethylaniline is used in<br />

the usual process for the manufacture <strong>of</strong> tetryl. <strong>The</strong> amount <strong>of</strong><br />

this impurity in the usual process depends upon the amount <strong>of</strong><br />

monomethylaniline which may be present. A large excess <strong>of</strong><br />

sulfuric acid tends toward the production <strong>of</strong> m-nitro compounds,<br />

but a reduction in the amount <strong>of</strong> sulfuric acid is not feasible for<br />

this increases the amount <strong>of</strong> benzene-insoluble material. m-Nitrotetryl<br />

reacts with water, as TNA does; the nitro group in the<br />

3-position is replaced by hydroxyl, <strong>and</strong> m-hydroxytetryl or<br />

2,4,6-trinitro-3-methylnitraminophenol, yellow crystals from<br />

water, m.p. 183°, is formed. This substance resembles picric acid<br />

<strong>and</strong> forms explosive salts. It is readily soluble in water, <strong>and</strong><br />

87 Van Romburgh, Rec. trav. chim., 8, 274 (1889). Van Romburgh <strong>and</strong><br />

Schepers, Versl. Kon. Akad. Wetenschapen, 22, 293 (1913), also prepared<br />

this substance by thje nitration <strong>of</strong> dimethylaniline (in 20 times its weight <strong>of</strong><br />

concentrated sulfuric acid).

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