Process for preparing diisocyanates based on lysine
The invention relates to a process for preparing a diisocyanate of the formula (A) where R is selected from the group consisting of alkyl, aryl, and combinations thereof, comprising the following process steps in the indicated order; 1) providing an intermediate of the formula (B) with a process using lysine and urea and where R and each R′ are independently selected from the group consisting of alkyl, aryl, and combinations thereof; and 2) thermolytic cleavage of the intermediate of the formula (B), thereby affording the diisocyanate of the formula (A), and also to the diisocyanate directly prepared therewith.
1. Process for preparing a diisocyanate of the formula (A)
where R is selected from the group consisting of alkyl, aryl, and combinations thereof, comprising the following process steps in the indicated order:
1) Providing an intermediate of the formula (B) with a process using lysine and urea
where R and each R′ are independently selected from the group consisting of alkyl, aryl, and combinations thereof; and
2) thermolytic cleavage of the intermediate of the formula (B),
thereby affording the diisocyanate of the formula (A); and
wherein the process further includes one of the following series of process steps prior to process step 1):
either a.1) providing of lysine;
a.2) reacting the lysine with urea to form a urea adduct of the formula (C)
and
a.3) reacting the urea adduct of the formula (C) with an alcohol to form the intermediate of the formula (B);
or b.1) providing of lysine;
b.2) reacting the lysine with a base to form a lysine salt of the formula (Z);
where X is a counterion;
b.3) reacting the lysine salt of the formula (Z) with urea to form a urea salt of the formula (Y);
where X is a counterion;
b.4) reacting the urea salt of the formula (Y) with an alcohol to form a carbamate of the formula (X)
where each R′ is independently selected from the group consisting of alkyl, aryl, and combinations thereof, and X is a counterion;
b.5) reacting the carbamate of the formula (X) with an acid to form the carboxylic acid of the formula (W)
where each R′ is independently selected from the group consisting of alkyl, aryl, and combinations thereof; and
b.6) reacting the carboxylic acid of the formula (W) with an alcohol to form the intermediate of the formula (B);
or c.1) providing of lysine;
c.2) reacting the lysine with a base to form a lysine salt of the formula (Z);
where X is a counterion;
c.3) reacting the lysine salt of the formula (Z) with urea to form a urea salt of the formula (Y);
where X is a counterion;
c.4) reacting the urea salt of the formula (Y) with an alcohol to form the intermediate of the formula (B).
2. Process according to claim 1 , wherein R is selected from the group consisting of C1-C8 alkyl.
3. Process according to claim 1 , wherein the thermolytic cleavage is mediated by a mediator.
4. Process according to claim 1 , wherein the process includes a further process step 3) after and/or during process step 2):
3) purifying the diisocyanate of the formula (A).
5. Process according to claim 1 , wherein the molar ratio of the urea in step a.2) is within a range from 1:1 to 5:1 based on the primary amine groups of the lysine, and the molar ratio of the urea in step b.3) or c.3) is within a range from 1:1 to 5:1 based on the primary amine groups of the lysine salt of the formula (Z).
6. Process according to claim 1 , wherein the pressure during the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is for at least part of the time within a range from ≥1 bar.
7. Process according to claim 6 , wherein the pressure during the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is within the specified range for 1 to 20 hours.
8. Process according to claim 1 , wherein the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is carried out at least at a temperature from 150 to 300° C.
9. Process according to claim 8 , wherein the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is conducted within the specified temperature range for a period of 1 to 20 hours.
10. Process according to claim 1 , wherein the molar ratio of the alcohol in step a.3) based on the urea adduct of the formula (C) is within a range from 2:1 to 100:1, the molar ratio of the alcohol in step b.6) based on the carboxylic acid of the formula (W) is within a range from 2:1 to 100:1, and the molar ratio of the alcohol in step c.4) based on the urea salt of the formula (Y) is within a range from 2:1 to 100:1.
11. Process according to claim 1 , wherein the reaction in process steps a.2), b.3) and c.3) is carried out in a polar solvent.
12. Process according to claim 2 , wherein R is selected from the group consisting methyl, ethyl, isopropyl, n-propyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
13. Process according to claim 3 , wherein the thermolytic cleavage is mediated by a metal-based catalyst.
14. Process according to claim 13 , wherein the metal-based catalyst is a tin(II) salt.
15. Process according to claim 4 , wherein the diisocyanate of the formula (A) is purified by fractional distillation.
16. Process according to claim 6 , wherein the pressure during the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is for at least part of the time within a range from 1 to 25 bar.
17. Process according to claim 7 , wherein the pressure during the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is within the specified range 4 to 6 hours.
18. Process according to claim 8 , wherein the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is carried out at least at a temperature from 190 to 220° C.
19. Process according to claim 9 , wherein the reaction with the alcohol in process step a.3), b.4), b.6), c.4) is conducted within the specified temperature range for a period of 4 to 6 hours.
20. Process according to claim 11 , wherein the polar solvent is water.