HETEROGENEOUS CATALYZED PROCESS FOR THE PRODUCTION OF 2,2,4,6,6-PENTAMETHYL-1,2,5,6-TETRAHYDRO-PYRIMIDINE

Abstract
The present invention relates to a process for the production of 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine comprising (i) providing a reactor containing a catalyst comprising a zeolitic material, wherein the zeolitic material comprises YO2 and optionally comprises X2O3 in its framework structure, wherein Y is a tetravalent element and X is a trivalent element; (ii) preparing a reaction mixture comprising acetone and ammonia; (iii) contacting the catalyst in the reactor with the reaction mixture prepared in (ii) for obtaining a reaction product comprising 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine; wherein the temperature programmed desorption of ammonia (NH3-TPD) profile of the zeolitic material comprised in the catalyst provided in (i) optionally displays one or more bands associated with medium acid sites, said one or more bands having maxima in the temperature range of from 250 to 500° C., wherein the integration of said one or more bands affords a total value of 0.5 mmol/g or less, and wherein the mixture prepared in (ii) and contacted with the catalyst in (iii) contains less than 10 wt.-% of water based on 100 wt.-% of the reaction mixture.
Description
Claims
  • 1. A process for the production of 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine comprising (i) providing a reactor containing a catalyst comprising a zeolitic material, wherein the zeolitic material comprises YO2 and optionally comprises X2O3 in its framework structure, wherein Y is a tetravalent element and X is a trivalent element;(ii) preparing a reaction mixture comprising acetone and ammonia; and(iii) contacting the catalyst in the reactor with the reaction mixture prepared in (ii) for obtaining a reaction product comprising 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine;wherein the temperature programmed desorption of ammonia (NH3-TPD) profile of the zeolitic material comprised in the catalyst provided in (i) displays one or more bands associated with medium acid sites, said one or more bands having maxima in the temperature range of from 250 to 500° C., wherein the integration of said one or more bands affords a total value of 0.5 mmol/g or less, andwherein the mixture prepared in (ii) and contacted with the catalyst in (iii) contains water in an amount in the range of from 0.01 to 10 wt.-% based on 100 wt.-% of the reaction mixture.
  • 2. The process of claim 1, wherein the NH3-TPD profile of the zeolitic material comprised in the catalyst provided in (i) displays one or more bands associated with medium acid sites, said one or more bands having maxima in the temperature range of from 250 to 500° C., wherein the integration of said one or more bands affords a total value of 0.45 mmol/g or less.
  • 3. The process of claim 1, wherein the NH3-TPD profile of the zeolitic material comprised in the catalyst provided in (i) displays one or more bands associated with strong acid sites, said one or more bands having maxima in the temperature range of from 510 to 800° C., wherein the integration of said one or more bands affords a total value of 0.05 mmol/g or less.
  • 4. The process of claim 3, wherein the one or more bands associated with strong acid sites have their maxima in the temperature range of from 530 to 750° C.
  • 5. The process of claim 1, wherein the integration of the bands in the NH3-TPD profile of the zeolitic material comprised in the catalyst provided in (i), said bands having maxima in the temperature range of from 50 to 800° C., affords a total value of 0.9 mmol/g or less.
  • 6. The process of claim 5, wherein the bands have their maxima in the temperature range of from 80 to 750° C.
  • 7. The process of claim 1, wherein the zeolitic material has a framework structure having a maximum ring size of 10 T-atoms or less.
  • 8. The process of claim 1, wherein Y is selected from the group consisting of Si, Sn, Ti, Zr, Ge, and mixtures of two or more thereof.
  • 9. The process of claim 1, wherein X is selected from the group consisting of B, Al, Ga, In, and mixtures of two or more thereof.
  • 10. The process of claim 1, wherein the zeolitic material has a YO2 : X2O3 molar ratio in the range of from 5 to 300.
  • 11. The process claim 1, wherein the zeolitic material provided in (i) comprises a zeolitic material having an MFI and/or an FER framework-type structure.
  • 12. The process of claim 1, wherein the process is conducted as a batch process or as a continuous process.
  • 13. The process of claim 1, wherein the process further comprises (iv) separating 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine from the reaction product to obtain 2,2,4,6,6-pentamethyl-1,2,5,6-tetrahydro-pyrimidine and a residual mixture; and(v) recycling at least a portion of the residual mixture in the reaction mixture in (ii).
  • 14. The process of claim 1, wherein in the reaction mixture prepared in (ii), the molar ratio of acetone to ammonia is in the range of from 1:1 to 25:1.
  • 15. The process of claim 1, wherein the catalyst is provided as a molding, wherein the molding is prepared according to a process comprising (a) preparing a mixture comprising the zeolitic material and optionally one or more binders;(b) shaping the mixture;(c) optionally drying the shaped material in a gas atmosphere; and(d) calcining the shaped material obtained from (b) or (c) in a gas atmosphere to obtain the molding.
Priority Claims (1)
Number Date Country Kind
20189315.3 Aug 2020 EP regional
PCT Information
Filing Document Filing Date Country Kind
PCT/EP2021/071729 8/4/2021 WO