Abstract: A process for the preparation of 2,2-dimethyl-4-cyano-butyraldoxime N-methyl-carbamate wherein 2,2-dimethyl-4-cyano-butyraldoxime is reacted with an at least equimolar amount of methylcarbamic acid chloride in the form of a concentrated solution of at least 8 moles thereof per liter of inert organic solvent, in the presence of from 1.05 to 2 moles of a tertiary aliphatic amine per mole of 2,2-dimethyl-4-cyano-butyraldoxime, at from 0.degree. to 30.degree. C.

Abstract: A novel process of preparing ketoxime carbamate by forming a halogenated intermediate which is reacted with an alkali metal compound and an isocyanate.

Abstract: An organic, substantially water-insoluble oxime product is recovered from the liquid reaction mixture of water, ammonium sulfate and the oxime product. First the reaction mixture is separated into a first liquid layer containing an aqueous ammonium sulfate solution and a second liquid layer containing an emulsion of the oxime product as the continuous phase and aqueous ammonium sulfate as the discontinuous phase. These layers are separated and the second liquid layer is contacted with solid ammonium sulfate for a time sufficient to agglomerate the discontinuous phase. The agglomerated discontinuous phase is then removed from the continuous phase. Thereafter, either a lites fraction can be distilled from the continuous phase or the oxime product can be distilled from the continuous phase, or both. The process is particularly applicable to the production of oximes such as Aldicarb oxime, cyclohexanone oxime and methylethylketoxime from aqueous reaction mixtures in which by-product ammonium sulfate is formed.

Abstract: An improved process for preparing an organic sulfone compound by oxidizing the corresponding sulfide compound with an aqueous peracid solution.

Abstract: A novel process of preparing ketoxime carbamate.