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Nitryl fluoride nitration with

The cr-complexes (iv) are thus the intermediates corresponding to the substitution process of hydrogen exchange. Those for some other substitutions have also been isolated in particular, benzylidyne trifluoride reacts with nitryl fluoride and boron trifluoride at — ioo°C to give a yellow complex. Above — 50 °C the latter decomposes to hydrogen fluoride, boron trifluoride, and an almost quantitative yield of tn-nitrobenzylidyne trifluoride. The latter is the normal product of nitrating benzylidyne trifluoride, and the complex is formulated as... [Pg.114]

Eremenko and co-workers used nitryl fluoride for the deamination of amines at subambient temperatures in acetonitrile. The same reaction occurs with primary nitramines and their alkali metal salts bis-nitramines react to give the corresponding bis-nitrate esters. [Pg.107]

Other reagents have been used for the direct nitration of amines under nonacidic conditions. Mandel reported the synthesis of methylnitramine, dimethylnitramine and diisopropy-Initramine from the reaction of nitryl fluoride with the parent amine. The presence of an excess of amine appears to be of prime importance given that other reports give the nitrosamine as a major by-product. [Pg.206]

Alkyl lV,lV-dinitramines (154) have been prepared from the reaction of the tetraalkylam-monium salts (155) of primary nitramines with nitryl fluoride in acetonitrile at subambient temperature. The same reaction with the primary nitramine or its alkali metal salts yields the corresponding nitrate ester. Treatment of the ammonium, potassium, or lithium salts of primary nitramines (156) with a solution of nitronium tetrafluoroborate in acetonitrile at subambient temperature yield alkyl iV,iV-dinitramines. ° The same reactions in ether or ester solvents enables the free nitramine to be used. The nitrolysis of A-alkylnitramides (157) and N,N-diacylamines with nitronium tetrafluoroborate in acetonitrile, and the nitration of aliphatic isocyanates with nitronium tetrafluoroborate and nitric acid in acetonitrile, also yield alkyl A,A-dinitramines (154). [Pg.287]

Deville first synthesized dinitrogen pentoxide in 1849 by reacting silver nitrate with chlorine gas. This reaction probably involves the initial formation of nitryl chloride and, accordingly, dinitrogen pentoxide can also be formed from the reaction of nitryl chloride or nitryl fluoride with a metal nitrate. These reactions are more of theoretical interest than of any practical value. [Pg.351]

K hydroxide can be fused using a mixt of Na hydroxide plus Na nitrate (Refs 7,49,50 55) W, in the finely divided state, is either spontaneously pyrophoric or reacts with gentle heating with a range of oxidants Air, Br trifluoride, Br pentafluoride. Cl trifluoride, fluorine, I pentafluoride, nitryl fluoride and oxygen di-fluoride (Refs 42 57)... [Pg.897]

Aluminum powder also forms sensitive explosive mixtures with oxidants such as liquid CI2 and other halogens, N2O4, tetranitromethane, bromates, iodates, NaC103, KCIO3, and other chlorates, NaN03, aqueous nitrates, KCIO4 and other perchlorate salts, nitryl fluoride, ammonium peroxodisulfate, sodium peroxide, zinc peroxide, and other peroxides, red phosphorus, and powdered pol)Ttetrafluoroethylene (PTFE). [Pg.44]

CADMIO (Spanish) or CADMIUM (7440-43-9) Cd Air exposure, especially of powdered form, may cause chemical to self-ignite. Finely divided material reacts violently with strong oxidizers, fused ammonium nitrate, bromine pentafluoride, lithium, nitryl fluoride, phosphorus trichloride, potassium chlorate carbon dioxide + heat, hydrozoic acid (possible explosion), nitric oxide, tellurium. Contact with acid forms explosive hydrogen gas. Contact with hexafluorobenzene forms a heat-sensitive explosive compound. May react with selenium, elemental sulfur, zinc. On small fires, use dry chemical powder (such as Puiple-K-Powder), foam, Halon, or CO2 extinguishers. [Pg.195]

ANTIMONY or ANTIMONY BLACK (7440-36-0) Dust or powder forms explosive mixture with air. Reacts violently with strong oxidizers and acids, especially halogenated acids, producing toxic stibine gas (antimony hydride). Reacts violently with anunonium nitrate, bromine, bromine azide, bromine tri fluoride, bromoazide, chloric acid, chlorine, chlorine monoxide, chlorine trifluoride, dichlorine oxide, disulfur dibromide, fluorine, halogens, iodine, iodine pentafluoride, nitrosyl fluoride, nitryl fluoride, potassium dioxide, potassium nitrate, potassium permanganate, potassium peroxide, sodium nitrate, sodium peroxide. Forms explosive V-chlorodimethylamines with chloric and perchloric acid. [Pg.123]

ARSENIC (7440-38-2) Finely divided material forms explosive mixture with air. Decomposes on contact with acids or acid fumes, emitting fumes of arsenic. Contact of dust or powder with strong oxidizers can cause ignition or explosion. Violent reaction with bromine azide, bromine pentafluoride, bromine trifluoride, dichlorine oxide, hypochlorous acid, nitrogen trichloride, tribromamine hexaammoniate, nitrogen oxyfluoride, potassium chlorate, potassium dioxide, powdered rubidium, silver fluoride. Incompatible with strong acids, cesium acetylene carbide, chromic acid, chromium trioxide, hafnium, halogens, lead monoxide, mercury oxide, nitryl fluoride, platinum, potassium nitrate, silver nitrate, sodium chlorate, powdered zinc. [Pg.132]

BENSULFOID (7704-34-9) Combustible solid (flash point 405°F/207°C). Finely divided dry materia forms explosive mixture with air. The vapor reacts violently with lithium carbide. Reacts violently with many substances, including strong oxidizers, aluminum powders, boron, bromine pentafluoride, bromine trifluoride, calcium hypochlorite, carbides, cesium, chlorates, chlorine dioxide, chlorine trifluoride, chromic acid, chromyl chloride, dichlorine oxide, diethylzinc, fluorine, halogen compounds, hexalithium disilicide, lampblack, lead chlorite, lead dioxide, lithium, powdered nickel, nickel catalysis, red phosphorus, phosphorus trioxide, potassium, potassium chlorite, potassium iodate, potassium peroxoferrate, rubidium acetylide, ruthenium tetraoxide, sodium, sodium chlorite, sodium peroxide, tin, uranium, zinc, zinc(II) nitrate, hexahydrate. Forms heat-, friction-, impact-, and shock-sensitive explosive or pyrophoric mixtures with ammonia, ammonium nitrate, barium bromate, bromates, calcium carbide, charcoal, hydrocarbons, iodates, iodine pentafluoride, iodine penloxide, iron, lead chromate, mercurous oxide, mercury nitrate, mercury oxide, nitryl fluoride, nitrogen dioxide, inorganic perchlorates, potassium bromate, potassium nitride, potassium perchlorate, silver nitrate, sodium hydride, sulfur dichloride. Incompatible with barium carbide, calcium, calcium carbide, calcium phosphide, chromates, chromic acid, chromic... [Pg.156]

COBALT (7440-48-4) An extreme fire hazard. Pyrophoric particles or dust can self-ignite in air. Violent reaction with acetylene, ammonium nitrate, bromine pentafluoride, bromine trifluoride, cumene hydroperoxide, hydrogen peroxide (90%), nitryl fluoride, organic peroxides forms explosive mixture with potassium chlorate. Incompatible with sodium borohydride. Capable of promoting the decomposition of many organic materials. [Pg.343]

ESTANO (Spanish) (7440-31-5) Finely divided material is combustible and forms explosive mixture with air. Contact with moisture in air forms tin dioxide. Violent reaction with strong acids, strong oxidizers, ammonium perchlorate, ammonium nitrate, bis-o-azido benzoyl peroxide, bromates, bromine, bromine pentafluoride, bromine trifluoride, bromine azide, cadmium, carbon tetrachloride, chlorine, chlorine monofluoride, chlorine nitrate, chlorine pentafluoride, chlorites, copper(II) nitrate, fluorine, hydriodic acid, dimethylarsinic acid, ni-trosyl fluoride, oxygen difluoride, perchlorates, perchloroethylene, potassium dioxide, phosphorus pentoxide, sulfur, sulfur dichloride. Reacts with alkalis, forming flammable hydrogen gas. Incompatible with arsenic compounds, azochloramide, benzene diazonium-4-sulfonate, benzyl chloride, chloric acid, cobalt chloride, copper oxide, 3,3 -dichloro-4,4 -diamin-odiphenylmethane, hexafluorobenzene, hydrazinium nitrate, glicidol, iodine heptafluoride, iodine monochloride, iodine pentafluoride, lead monoxide, mercuric oxide, nitryl fluoride, peroxyformic acid, phosphorus, phosphorus trichloride, tellurium, turpentine, sodium acetylide, sodium peroxide, titanium dioxide. Contact with acetaldehyde may cause polymerization. May form explosive compounds with hexachloroethane, pentachloroethane, picric acid, potassium iodate, potassium peroxide, 2,4,6-trinitrobenzene-1,3,5-triol. [Pg.503]


See other pages where Nitryl fluoride nitration with is mentioned: [Pg.710]    [Pg.711]    [Pg.790]    [Pg.214]    [Pg.1353]    [Pg.251]    [Pg.376]    [Pg.857]    [Pg.984]    [Pg.109]    [Pg.214]    [Pg.89]    [Pg.94]    [Pg.275]    [Pg.558]    [Pg.627]    [Pg.646]    [Pg.940]    [Pg.950]    [Pg.969]    [Pg.975]    [Pg.1008]    [Pg.1096]    [Pg.125]    [Pg.132]    [Pg.196]    [Pg.346]    [Pg.348]    [Pg.623]   
See also in sourсe #XX -- [ Pg.6 , Pg.109 ]

See also in sourсe #XX -- [ Pg.109 ]

See also in sourсe #XX -- [ Pg.6 , Pg.109 ]

See also in sourсe #XX -- [ Pg.109 ]




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Nitration nitryl fluoride

Nitryl fluoride

With fluoride

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