Hydrogen with iodine monochloride

Consider the gas-phase reaction of hydrogen with iodine monochloride to form hydrogen chloride and iodine. 

The synthesis of ionic triiodinated contrast agents starts from either bisamino nitrophthalic acid or amino isophthalic acid. The nitro group is reduced to the amino moiety by hydrogenation. Iodine is introduced in aqueous solution with iodine monochloride. Due to the decrease in solubiHty the resulting triiodobenzene precipitates from the solution and can be recrystallised. Amino functions are then acylated. 

An alcoholic solution of iodine is decolorised by arsine, some arsenious acid being formed in solution, and after passing the gas for some time a black precipitate appears.4 Admixture of arsine with hydrogen chloride results in the formation of a brown cloud of arsenic 5 aqueous hydrochloric acid and arsine yield arsenic trichloride.6 Arsine reacts quantitatively with iodine monochloride in aqueous solution with liberation of iodine, thus ... 

Compound 85 was dehydrogenated at 300° over palladium black under reduced pressure to a pyridine derivative 96 which was independently synthesized by the following route. Anisaldehyde (86) was treated with iodine monochloride in acetic acid to give the 3-iodo derivative 87. The Ullmann reaction of 87 in the presence of copper bronze afforded biphenyldialdehyde (88). The Knoevenagel condensation with malonic acid yielded the unsaturated diacid 91. The methyl ester (92) was also prepared alternatively by a condensation of 3-iodoanisaldehyde with malonic acid to give the iodo-cinnamic acid (89), followed by the Ullmann reaction of its methyl ester (90). The cinnamic diester was catalytically hydrogenated and reduced with lithium aluminium hydride to the diol 94. Reaction with phosphoryl chloride afforded an amorphous dichloro derivative (95) which was condensed with 2,6-lutidine in liquid ammonia in the presence of potassium amide to yield pyridine the derivative 96 in 27% yield (53). 

The value of Gtotalgas was found to be 0.87 [385]. Methane and hydrogen are the main products [386, 387]. A new absorption at 11.25 pm, assigned to vinylidene double bonds, was observed [386]. Total unsaturation was measured by titration with iodine monochloride. It corresponds to the formation of 1.87 double bonds per main-chain scission irrespective of temperature. Main-chain scissions were determined at various temperatures (Table 28). An Arrhenius-type plot of Gscission versus temperature gives an activation energy of 2.5 kcal mole-1 above 0°C. Below 0°C, the temperature coefficient is negligible. 

LEAD SULFIDE (1314-87-0) PbS Noncombustible solid. Reacts violentiy with iodine monochloride, hydrogen peroxide. Incompatible with bromates, chlorates, hydrazinium nitrate, iodates, mercurous chloride, silver azide, zinc(II) nitrate, hexahydrate. 

Most chemical reactions do not occur in a single step, but over the course of several steps. When we write a chemical equation to represent a chemical reaction, we usually represent the overall reaction, not the series of individual steps by which the reaction occurs. Consider the reaction in which hydrogen gas reacts with iodine monochloride ... 

Organoborane intermediates can also be used to synthesize alkyl halides. Replacement of boron by iodine is rapid in the presence of base.150 The best yields are obtained with sodium methoxide in methanol.151 If less basic conditions are desirable, the use of iodine monochloride and sodium acetate gives good yields.152 As is the case in hydroboration-oxidation, the regioselectivity of hydroboration-halogenation is opposite to that observed for direct ionic addition of hydrogen halides to alkenes. Terminal alkenes give primary halides. 

Iodine trichloride.—This compound was discovered by J. L. Gay Lussac as the result of treating warm iodine or iodine monochloride with an excess of chlorine. The trichloride collects as a citron-yellow crystalline sublimate on the cooler parts of the vessel. It is also formed by the action of liquid chlorine on iodine, or an iodide—say lead iodide.18 The iodine trichloride is almost insoluble in liquid chlorine, and hence, say Y. Thomas and P. Dupuis, this method of preparation is very convenient. It is also formed by the action of dry chlorine on hydrogen iodide (A. Christomanos) silver iodate (J. Krutwig) or methyl iodide (L. von... 

Monosubstitution of the free amine may be achieved by using a less reactive electrophile. Thus aniline and o-toluidine may be mono-iodinated (Expt 6.60) by treatment with iodine (in the presence of sodium hydrogen carbonate or calcium carbonate to remove the liberated hydrogen iodide), the substituent entering the position para to the amino group. Direct iodination can also be effected by using the more powerfully electrophilic reagent, iodine monochloride... 

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. 

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