Method for producing methacrolein and the conditioning/draining thereof for direct oxidative esterification

Patent metadata

Field	Value
Publication number	US-9580374-B2
Application number	US-201414916440-A
Country	US
Kind code	B2
Filing date	Aug 27, 2014
Priority date	Sep 26, 2013
Publication date	Feb 28, 2017
Grant date	Feb 28, 2017

Abstract

The present invention relates to a process for preparing methyl methacrylate by direct oxidative esterification of methacrolein and the preparation of methacrolein. It is a feature of this novel process that it was possible to distinctly increase the yield and the efficiency of the process compared to the prior art through a sequence of different distillation steps.

First claim

The invention claimed is:

1. A process for preparing methyl methacrylate, comprising the steps of:
A) preparing methacrolein from propanal and formaldehyde in the presence of amine salts;
B) isolating liquid crude methacrolein by distillation in a first distillation column and subsequently separating from an aqueous phase;
C) distilling the crude methacrolein obtained from step B) in a second distillation column in the presence of methanol;
D) subsequently oxidatively esterifying the methacrolein obtained from step C) with methanol and oxygen in the presence of a heterogeneous noble metal-containing oxidation catalyst comprising metals and/or metal oxides in a reactor; and
E) distilling the product obtained from step D) in a distillation column, and recycling a distillate comprising methacrolein and methanol into the reactor of step D).

2. The process according to claim 1 , wherein the distillation columns of steps C) and E) are the same distillation column.

3. The process according to claim 2 , wherein a mixture of methanol and methacrolein from the distillation column of step E) is recycled into the reactor of step D), and further methanol is optionally added to the second distillation column in step E).

4. The process of claim 2 , wherein a substream of the crude methacrolein from step B) is passed into the reactor of step D), and in that the ratio of this substream to the stream from the distillation column of step E) into the reactor of step D) is between 1:2 and 1:20.

5. The process of claim 1 , wherein in process step C) or B), dimethacrolein is removed together with the column bottoms and an amount of dimethacrolein less than the amount in the stream which is introduced from process step B) into process step C) is introduced into process step D).

6. The process of claim 1 , wherein the heterogeneous oxidation catalyst used for the oxidative esterification reaction in step D) comprises one or more ultrafinely divided metals having an average particle size of <20 nm, selected from the group consisting of gold, palladium, ruthenium, rhodium and silver, and in that the reaction in step D) is conducted at a pressure of 1 to 100 bar in the liquid phase.

7. The process of claim 1 , wherein the conversion in step D) is conducted at a pressure in the range from 2 to 50 bar and at a temperature in the range from 10 to 200° C. in the liquid phase.

8. The process of claim 1 , wherein in the distillation column of step E), a low boiler stream comprising methyl formate is removed overhead and disposed of.

9. The process of claim 1 , wherein the oxidative esterification reaction in step D) is effected with a molar ratio of methanol to methacrolein in the range from 1:1 to 50:1.

10. The process of claim 1 , wherein steps A) to E) are conducted in a continuous process.

11. The process of claim 1 , wherein the bottoms from the second distillation column of step E) are transferred into an extraction in which water is used to separate the stream into an organic phase and an aqueous phase.

12. The process of claim 1 , wherein the bottoms from the second distillation column of step E) are transferred into a phase separator and separated therein into an organic phase and an aqueous phase.

13. The process of claim 11 , wherein the respective organic phase is purified further in at least one further distillation step.

14. The process of claim 1 wherein the stream from step C) or E), comprising methanol and methacrolein, passed into the reactor of step D) includes an amount of water less than the amount of water in the crude methacrolein from step B).

15. The process of claim 1 , wherein the separation from the aqueous phase after step B) is effected in a phase separator.

16. The process of claim 1 , wherein the conversion in process step A) is conducted in the presence of 0.1 to 20 mol % of organic base, and 0.1 to 20 mol % of acid, based in each case on the propanal, at a temperature of 100 to 300° C. and at a pressure of 5 to 100 bar.

Assignees

• Krill Steffen
• Groemping Matthias
• Lygin Alexander
• Balduf Torsten
• Burghardt Rudolf
• Evonik Roehm Gmbh

Inventors

• Krill Steffen
• Groemping Matthias
• Lygin Alexander
• Balduf Torsten
• Burghardt Rudolf

Classifications

• C07C67/39

  by oxidation of groups which are precursors for the acid moiety of the ester · CPC title

• C07C45/84

  by azeotropic distillation · CPC title

• C07C45/75 Primary

  Reactions with formaldehyde · CPC title

• C07C69/54

  Acrylic acid esters; Methacrylic acid esters · CPC title

• C07C45/82

  by distillation · CPC title