Process for preparing isocyanates containing alkoxysilane groups

Patent metadata

Field	Value
Publication number	US-10669293-B2
Application number	US-201916356081-A
Country	US
Kind code	B2
Filing date	Mar 18, 2019
Priority date	Mar 28, 2018
Publication date	Jun 2, 2020
Grant date	Jun 2, 2020

Abstract

The present invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D),
A) alkoxysilanoalkylamine is reacted with urea in the presence of an alcohol, optionally in the presence of at least one catalyst, to give alkoxysilanoalkylurethane, B) simultaneously or successively, if used, the catalyst is removed and/or deactivated, and low boilers, medium boilers and/or high boilers are removed, C) purified alkoxysilanoalkylurethane is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, in which, in step C),
i) the bottoms material is wholly or partly discharged from the cleavage apparatus, ii) subjected to thermal treatment and/or purification and/or an aftertreatment in the presence of alcohol and iii) the material removed, after thermal treatment and/or purification and/or aftertreatment in step B) or C), is fed in again.

First claim

The invention claimed is:

1. A process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D),
A) reacting an alkoxysilanoalkylamine with urea in the presence of an alcohol, optionally in the presence of at least one catalyst, to give alkoxysilanoalkylurethane,
B) simultaneously or successively producing purified alkoxysilanoalkylurethane by
removing or deactivating the catalyst, and
removing low boilers, medium boilers and/or high boilers,

C) thermally cleaving the purified alkoxysilanoalkylurethane in a cleavage apparatus to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material of the cleaving the purified alkoxysilanoalkylurethane, wherein the bottoms material of the cleaving the purified alkoxysilanoalkylurethane is wholly or partly discharged from the cleavage apparatus, and
D) separating the isocyanate containing alkoxysilane groups and by-product from one another and from bottoms material and collected,
wherein
i) the bottoms material is wholly or partly discharged from the cleavage apparatus,
ii) subjected to thermal treatment and/or purification and/or an aftertreatment in the presence of alcohol and
iii) the material removed, after thermal treatment and/or purification and/or aftertreatment in step B) or C), is fed in again.

2. The process according to claim 1 , wherein the alkoxysilanoalkylamine has the formula (1)
R a m (OR 2 ) 3-m Si—R 1 —NH 2   (1)

where R 3 , R 2 and R 1 are each independently identical or different hydrocarbyl radicals having 1-6 carbon atoms, where these may be linear, branched or cyclic, and m is 0-2 and step C) is conducted without solvent and in the presence of a catalyst at a temperature of 140-280° C. and a pressure of 0.5-200 mbar.

3. The process according to claim 2 , wherein in step B), in the sequence of steps i) to iv),
i) removing or deactivating the catalyst,
ii) removing low boilers, medium boilers and/or high boilers in three separate component steps by removing the low boilers via flash evaporation,
iii) removing the medium boilers via falling-film evaporation or thin-film evaporation and
iv) removing the high boilers via short-path evaporation or thin-film evaporation.

4. The process according to claim 3 , wherein low and medium boilers removed are recycled into the urethane synthesis A).

5. The process according to claim 2 , wherein the urea used is unconditioned.

6. The process according to claim 2 , wherein the alcohol has the formula (2)
R 4 —OH  (2)

where R 4 is a linear, branched or cyclic hydrocarbyl radical having 1-6 carbon atoms.

7. The process according to claim 2 , wherein the alkoxysilanoalkylamine is used together with urea and alcohol in a molar ratio of these three components of 1:1.01:3.0 to 1:1.5:10.

8. The process according to claim 2 , wherein in step A), ammonia formed during the reaction is removed.

9. The process according to claim 1 , wherein the urea used is unconditioned.

10. The process according to claim 1 , wherein the alcohol has the formula (2)
R 4 —OH  (2)

where R 4 is a linear, branched or cyclic hydrocarbyl radical having 1-6 carbon atoms.

11. The process according to claim 1 , wherein alkoxysilanoalkylamine is used together with urea and alcohol in a molar ratio of these three components of 1:1.01:3.0 to 1:1.5:10.

12. The process according to claim 1 , wherein in step A), ammonia formed during the reaction is removed.

13. The process according to claim 1 , wherein the thermal cleavage C) is conducted without solvent and in the presence of a catalyst at a temperature of 160-260° C. and a pressure of 1.0-100 mbar, and wherein the catalyst concentration is 0.5-255 ppms.

14. The process according to claim 13 , wherein the catalyst concentration is 1-100 ppm.

15. The process according to claim 1 , wherein, in step C), an amount of bottoms material corresponding to 1-90% by weight based on the feed is discharged from the bottom and added again in step B) or C).

16. The process according to claim 1 , wherein the discharged bottoms material
is subjected to thermal treatment at a temperature of 190-290° C. over a period of 0.2 to 4 h and/or
is distilled under reduced pressure and at a temperature of 190-290° C. and/or
is converted in the presence of an alcohol of the formula R 2 OH with R 2 =linear, branched or cyclic hydrocarbyl radical having 1-6 carbon atoms at 25-100° C. in the presence or absence of a catalyst.

17. The process according to claim 16 , wherein no reaction with alcohol is conducted.

18. The process according to claim 1 , wherein the separation in step D) is a rectification.

19. The process according to claim 18 , wherein the isocyanate obtained after the rectification is additionally purified by distillation.

20. The process according to claim 1 , wherein from 5 to 60% by weight based on the feed of bottoms material of the cleaving the purified alkoxysilanoalkylurethane is discharged from the cleavage apparatus.

Assignees

• Evonik Degussa Gmbh
• Evonik Operations Gmbh

Inventors

• Kreczinski Manfred
• Kohlstruk Stephan
• Hoppe Dirk
• Spyrou Emmanouil

Classifications

• C07F7/1892

  by reactions not provided for in C07F7/1876 - C07F7/1888 · CPC title

• C07F7/1804 Primary

  Compounds having Si-O-C linkages (Si-O-acyl linkages C07F7/1896) · CPC title

• C07F7/20 Primary

  Purification, separation · CPC title