Abstract:
A tertiary amine is effectively prepared by reacting a primary or secondary amine with formaldehyde in the presence of a palladium or platinum catalyst at a hydrogen pressure of 3 to 50 kg/cm2 (gauge pressure) at a temperature of 80.degree. to 180.degree. C., by controlling the addition of formaldehyde to the starting amine.
Abstract translation:在钯或铂催化剂的存在下,在氢压为3〜50kg / cm 2(表压)下,在80〜180℃的温度下,使伯胺或仲胺与甲醛反应,可有效制备叔胺。 ,通过控制向起始胺中加入甲醛。
Abstract:
A tertiary amine of a high purity is prepared from an alcohol or an aldehyde and a primary or second amine at a low temperature, using a catalyst of copper, nickel and an element belonging to the VIII platinum group such as platinum, palladium, ruthenium and rhodium, while removing out water formed by the reaction.
Abstract:
A process for the manufacture of aminopolyols and polyaminopolyols by continuous reductive amination of sugars in aqueous solution is described. Syrups such as corn syrups may be used directly for this process. It has been found that the lower the mol ratio of NH.sub.3 to the sugar, with a ratio of 1 as the lower limit, the higher is the degree of nitrogen incorporation into the sugar. It is essential that the streams of ammonia and aqueous sugar solution be pumped to the reaction zone separately.
Abstract:
Process for preparing cyclic amines by the reductive amination of saturated cyclic ketones. For example, cyclohexanone is reductively aminated to obtain N,N-dimethylcyclohexylamine.
Abstract:
A process for producing aliphatic amines which comprises reacting an aliphatic alcohol or an aliphatic aldehyde with an aminating agent selected from the group consisting of ammonia, a primary amine and a secondary amine in the liquid phase in the presence of an unsupported catalyst consisting essentially of (1) copper oxide or copper hydroxide and (2) a Group II A metal oxide or hydroxide. In a preferred embodiment the catalyst system also contains an organo nickel compound.
Abstract:
This invention concerns the synthesis of linear alkyl primary amines from a-olefins via an oxoamination process comprising (a) hydrogen and carbon monoxide addition to olefinic substrates to obtain aldehyde-containing compounds in the presence of ligand-stabilized platinum(II) halide catalysts with Group IVB metal halide cocatalysts, and (b) reductive amination of said aldehydic intermediates in the presence of oxide-supported, nickel catalysts.
Abstract:
Tertiary monomethylamines having long chain alkyl groups are advantageously prepared from unsaturated aliphatic nitriles under a low pressure at a high yield by the steps of:(a) reducing the nitriles with hydrogen in the presence of a nickel hydrogenation catalyst at 200.degree. through 230.degree. C. and under a hydrogen pressure of 0 through 10 kg/cm.sup.2 G, while the formed ammonia is removed;(b) reacting the resultant amines with a hydroxymethylation agent in the presence of the nickel catalyst at 150.degree. through 180.degree. C., while hydrogen is passed through the reaction zone under 0.3 through 7 kg/cm.sup.2 G and the formed water is removed, and;(c) reducing the resultant tertiary amines with hydrogen in the presence of the nickel catalyst at 175.degree. through 210.degree. C. and under a hydrogen pressure of 5 through 10 kg/cm.sup.2 G.
Abstract:
A two-step process for the production of aliphatic or cycloaliphatic diamines having 4 to 18 carbon atoms is disclosed wherein in the first step an aliphatic or cycloaliphatic dialdehyde is reacted with a monoamine olefin at atmospheric pressure at a temperature up to 100.degree. C. to form the corresponding diazomethyne and in the second step the diazomethyne is reacted at 60.degree. to 200.degree. C. and 50 to 300 bar with a mixture of ammonia and hydrogen in the presence of a hydrogenation catalyst to form the corresponding diamine and release of monoamine.
Abstract:
An improved process for the preparation of asymmetrical N-phenyl-N'-substituted para-phenylene diamines by the reductive alkylation of para-nitroso-diphenylhydroxylamine with an aldehyde or a ketone in the presence of hydrogen and a hydrogenation catalyst is disclosed. The improvement comprises utilizing as the hydrogenation catalyst (1) one member selected the group consisting of palladium and platinum sulfide, in an amount less than 1%, by weight, based on the weight of para-nitroso-diphenylhydroxylamine, and (2) activated carbon with a specific surface area of at least 700 square meters per gram and an ash content of less than 7.5%, by weight.
Abstract:
Covers a method of preparing diaminodiphenylmethanes and higher homologues thereof which comprises the step of condensing aniline and formaldehyde in the presence of an aluminum silicide catalyst.