Process for the ozonolysis of unsaturated compounds
A process for the ozonolysis of unsaturated starting materials, which is characterized in that the reaction is carried out in a structured reactor.
1. A process for the preparative ozonolysis of unsaturated starting materials, comprising reacting unsaturated compounds selected from the group consisting of aliphatic C 4 -C 40 hydrocarbons, C 4 - C 40 monocarboxylic acids, esters of C 1 -C 10 alcohols or polyols with C 4 -C 40 monocarboxylic acids, C 4 -C 40 dicarboxylic acids, and esters of C 1 -C 10 alcohols or polyols with C 4 -C 40 dicarboxylic acids, with ozone in a microreaction system applied to a support, wherein said support comprises 10 to 1000 microreaction channels running parallel to one another, which channels may be actuated sequentially or simultaneously with the starting materials, to form ozonization products, wherein said unsaturated compounds contain 1 to 4 double bonds, and wherein said ozonization products are immediately subjected to oxidative cleavage by using an oxygen-containing gas stream, or, alternatively, to reductive cleavage by using a hydrogen-containing gas stream.
2. The process of claim 1 , wherein the reaction channel diameter of said microreaction system does not exceed the limiting gap width.
3. The process of claim 1 , wherein said microreaction system has at least one inlet for the starting materials and at least one outlet for the products.
4. The process of claim 1 , wherein said support comprises a silicon/glass composite.
5. The process of claim 1 , wherein said microreaction system is applied to said support by suitable microstructuring techniques.
6. The process of claim 1 , wherein said microreaction channels have the same or different geometries.
7. The process of claim 1 , wherein said microreaction channels have measurements of from 50 to 1500 μm in at least one spatial direction.
8. The process of claim 1 , wherein said microreaction channels have a depth of from 20 to 1800 μm.
9. The process of claim 1 , wherein said microreaction channels have cross-sections of about 400 μm 2 to about 2.7×10 −6 m 2 .
10. The process of claim 1 , wherein said microreaction system comprises channels with a length of 1 to 1000 mm.
11. The process of claim 1 , wherein said microreaction channels have one or more mixing zones, one or more reaction zones, one or more mixing and reaction zones, one or more heating or cooling zones, or any combinations thereof.
12. The process of claim 1 , wherein said ozonolysis is carried out at a temperature in the range of −40° C. to 60° C.
13. The process of claim 1 , wherein said ozonolysis is carried out in the absence of pressure, or under a pressure in the range of 1 to 25 bar.
14. The process of claim 1 , wherein said ozonolysis is carried out with an ozone-containing gas mixture.
15. The process of claim 1 , wherein, following ozonization of said unsaturated starting materials to create ozonization products, said ozonization products are subjected to oxidative cleavage, which is carried out in the presence of suitable catalysts at a temperature in the range of from 20° C. to 140° C.
16. The process of claim 15 , wherein said oxidative cleavage of said ozonization products is carried out under a pressure in the range of 1 to 10 bar.
17. The process of claim 1 , wherein, following ozonization of said unsaturated starting materials to create ozonization products, said ozonization products are subjected to reductive cleavage, which is carried out in the presence of one or more suitable catalysts at a temperature in the range of from 20° C. to 100° C.
18. The process of claim 17 , wherein said reductive cleavage of said ozonization products is carried out under a pressure in the range 1 to 10 bar.
19. The process of claim 1 , wherein, following ozonization of the unsaturated starting materials to create ozonization products, said ozonization products are subjected to oxidative cleavage, then to reductive cleavage in the same microreaction system.
20. A process for the decomposition of ozonides in a microreaction system, compromising subjecting said ozonides to oxidative cleavage at a temperature in the range of from 20° C. to 140° C. in the absence of pressure, or at a pressure in the range of from about 1to about 10 bar, in the presence of one or more catalysts, followed by reductive cleavage at a temperature of from 20° C. to 100° C. in the absence of pressure, or at a pressure in the range of from about 1 to about 10 bar, in the presence of one or more catalysts.