Abstract:
A process for the preparation of o-nitrobenzaldehyde, comprising converting to the corresponding acetals a mixture of nitrated benzaldehyde which contains about 10 to 30% of o-nitrobenzaldehyde and about 70 to 90% of m-nitrobenzaldehyde, removing the o-nitrobenzaldehyde acetal by distillation, and then converting the o-nitrobenzaldehyde acetal to o-nitrobenzaldehyde.
Abstract:
To obtain technical TRIFLURALIN with a nitrosoamine content not exceeding 1 ppm, for use as a herbicide, 1-chloro-2,6-dinitro-4-(trifluoromethyl) benzene (DINITRO-PCBT) is freed from nitrosating agents by a process in which DINITRO-PCBT is treated with an aqueous bisulphite solution having an SO.sub.2 concentration of between 1% and 5% at a pH of between 1 and 3, at a temperature of between 50.degree. and 100.degree. C. for a time of between 1 and 3 hours. The organic layer is then separated from the aqueous layer, and the acidity and last traces of the bisulphite solution are eliminated from the organic layer by means of an aqueous alkaline solution.
Abstract:
Crude phenoxybenzoic acid herbicide, e.g., acifluorfen, having one or more undesirable isomers/by-product impurities associated therewith is separated therefrom employing an inert solvent which is selective for the isomers/other by-products.
Abstract:
The invention relates to a method of eliminating or substantially reducing the amount of cyanide formed in a polynitroaromatic, e.g. dinitrotoluene process. The invention comprises removing the nitrophenolic material from the mononitroaromatic formed in a first stage nitration of toluene prior to feeding the mononitroaromatic to the subsequent nitration zones.
Abstract:
A high melting, high boiling organic compound is easily and stably purified by continuously supplying the molten organic compound to a rectification zone under a subatmospheric pressure and continuously distilling off and recovering vapors from the top of the rectification zone, while continuously withdrawing bottoms containing higher boiling impurities and/or involatile impurities than the desired compound from a reboiling zone at the bottom of the rectification zone to the outside of rectification system by means of a barometric leg, without any pretreatment of removing lower boiling impurities therefrom before the rectification, and without disturbing a pressure balance in the rectification system.
Abstract:
In the nitration of a volatile aromatic compound wherein the compound is reacted with a liquid nitrating agent thereby to effect nitration and to produce a waste gas containing some of the aromatic compound, nitrogen oxides and nitric acid, the improvement which comprises contacting the waste gas with fresh nitrating agent thereby to remove the aromatic compound from the gas into the nitrating agent, and thereafter using such nitrating agent to effect subsequent nitration.
Abstract:
A novel improved process for separating mixtures of 3- and 4-nitrophthalic acid is described. The said process comprises treating a mixture of 3- and 4-nitrophthalic acid, which mixture is free from inorganic acid residues, in an aqueous-organic medium containing 1-20 percent by volume of water, at a temperature of between 20.degree. and 100.degree. C., stepwise with a base capable of forming salts of 3- and 4-nitrophthalic acid, which salts are essentially insoluble in the reaction medium, the treatment being carried out by adding base until a pH value of about 2.8 is obtained, separating the precipitating product consisting mainly of a 3-nitrophthalic acid mono-salt, subsequently precipitating, by the addition of further base, a product consisting principally of a 4-nitrophthalic acid salt, and finally converting the resulting nitrophthalic acid salts separately into the corresponding free acids, and optionally purifying these. The 3- and 4-nitrophthalic acid can be obtained by the process according to the invention in a simple manner in an isomer-free form and in good to very good yields.
Abstract:
The production of 2,2',4,4',6,6'-hexanitrostilbene-I (HNS-I) having finelyivided particles of uniform size by dissolving HNS-II in hot fuming nitric acid and then drowning the HNS-nitric acid solution in water.
Abstract:
The wash liquor resulting from the nitration of aromatic compounds is contacted with a quantity of the same aromatic compound being nitrated and the resultant solution is recycled to the nitration process.
Abstract:
An inclusion compound comprising meta-cyclophane of the formula ##STR1## and at least one benzene derivative included therein. And a process for separating an isomer containing a substituent at least at the 1- and 4-positions from a mixture containing isomers of a benzene derivative, which comprises contacting the meta-cyclophane with the mixture containing isomers of a benzene derivative thereby to form an inclusion compound in which an isomer containing a substituent at least at the 1- and 4-positions is included in the meta-cyclophane, then separating the inclusion compound from the mixture, and thereafter separating the isomer from the inclusion compound.