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Methylmethacrylates from acetone

The ACH process has recently been improved, as stated by Mitsubishi Gas. Acetone-cyanohydrin is first hydrolized to 2-hydroxyisobutylamide with an Mn02 catalyst the amide is then reacted with methylformiate to produce the methyl ester of 2-hydroxyisobutyric acid, with coproduction of formamide (this reaction is catalyzed by Na methoxide). The ester is finally dehydrated with an Na-Y zeolite to methylmethacrylate. Formamide is converted to cyanhydric acid, which is used to produce acetone-cyanohydrin by reaction with acetone. The process is very elegant, since it avoids the coproduction of ammonium bisulphate, and there is no net income of HCN. Problems may derive from the many synthetic steps involved, and from the high energy consumption. [Pg.267]

In the petrochemical industry the introduction of unsaturations in hydrocarbons is mainly obtained by dehydrogenation. This kind of reaction is less suitable for the functionalization of fine chemicals, because the high temperature necessary for the endothermic reaction can lead to the decomposition of thermally unstable compounds. An alternative reaction consists in the oxidative dehydrogenation, that can be carried out at lower temperatiu es. An example of this kind of reaction is constituted by the synthesis of methacrylic add (MAA, intermediate of methylmethacrylate production) via the oxidative dehydrogenation of isobutyric add (IBA), itself obtained from isobutyraldehyde (by-product of the oxo synthesis of nbutyraldehyde from propylene). This process constitutes one of the economically most interesting routes, alternative to the acetone-cyanohydrin process, which nowadays is the predominant process for the MAA production. [Pg.471]

The current industrial production of methylmethacrylate by the acetone-cyanohydrin process suffers from a number of drawbacks, which make it environmentally unfriendly. In particular, it makes use of a very toxic reactant (HCN) and intermediate (acetone cyanohydrin), and coproduces large amounts of impure ammonium sulphate, contaminated with organic compounds. Among the several alternative synthetic routes which have been proposed, particularly interesting from both the practical and scientific points of view is the single-step oxidation of isobutane to methacrylic acid, intermediate in the synthesis of methylmethacrylate. Several industrial companies have studied this reaction (and the selective oxidation of propane to acrylic acid, as well), and it has been established that the most active and selective catalysts are those which are based on Keggin-type polyoxometalates (POM s), containing phosphorus and molybdenum as the main components [1-18]. [Pg.141]

The oligomer components from 10-mer to 59-mer separated completely. The amount of the sample injected on the silica gel column was 50 mg (100 pi of 50 w/v% acetone solution). SFC separation of the methylmethacrylate (MMA) oligomer with a DP of 9.9 was performed. [Pg.298]


See other pages where Methylmethacrylates from acetone is mentioned: [Pg.217]    [Pg.171]    [Pg.267]    [Pg.553]    [Pg.5]   
See also in sourсe #XX -- [ Pg.231 ]




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