Processes for converting glycerol to amino alcohols

• US 20070287868A1
• Filed: 06/07/2007
• Published: 12/13/2007
• Est. Priority Date: 06/07/2006
• Status: Active Grant

• Current Assignee: The Procter & Gamble Company
• Original Assignee: The Procter & Gamble Company
• Inventors: Corrigan, Patrick, Gibson, Michael, Arredondo, Victor, Cearley, Angella, Back, Deborah, Fairweather, Neil
• Granted Patent: US 7,619,119 B2
• Time in Patent Office: Days
• US Class Current: 564/479
• CPC Class Codes: C07C 215/08 with only one hydroxy group and one amino group bound to the carbon skeleton

Abstract

Processes for converting glycerol to an amino alcohol product involving reacting glycerol with a metal catalyst to obtain hydroxyacetone, and reacting the hydroxyacetone with an amine compound to obtain an adduct that is then reduced using a reducing agent to obtain an amino alcohol product are described.

Claims

1. A process for converting glycerol to an amino alcohol product comprising:

reacting glycerol with a metal catalyst to obtain hydroxyacetone;

reacting the hydroxyacetone with an amine compound to obtain an adduct; and

reducing the adduct using a reducing agent to obtain an amino alcohol product.

2. The process of claim 1, wherein the metal catalyst is a catalyst selected from the group consisting of copper, chromium, nickel, zinc, cobalt, manganese, silicon, aluminum, copper chromite, copper zinc, oxides thereof, and combinations of any thereof.

3. The process of claim 1, wherein reacting the glycerol with the metal catalyst occurs at a temperature of from about 160°

C. to about 300°

C.

4. The process of claim 1, wherein reacting the glycerol with the metal catalyst occurs under gas sparging.

5. The process of claim 1, wherein reacting the glycerol with the metal catalyst occurs at a pressure of from about 0.1 bar to about 60 bar.

6. The process of claim 1, wherein the reducing agent comprises hydrogen in the presence of a hydrogenation catalyst selected from the group consisting of nickel, cobalt, RANEY®

nickel, RANEY®

cobalt, RANEY®

nickel or RANEY®

cobalt doped with other transition metals, nickel oxide, copper, palladium, platinum, rhodium, ruthenium, chromium, iridium, rhenium, manganese, molybdenum, iron, titanium, zirconium, magnesium, oxides thereof, and combinations of any thereof.

7. The process of claim 6, wherein the hydrogen is at a pressure of from about 1 bar to about 350 bar.

8. The process of claim 6, wherein the hydrogenation catalyst is supported on a material selected from the group consisting of alumina, titania, zirconia, charcoal, chromia, silica, zeolites, and combinations of any thereof.

9. The process of claim 1, wherein the amine compound is a compound selected from the group consisting of ammonia, ammonium hydroxide, hydroxylamine, primary amines, secondary amine, alkanolamines and combinations of any thereof.

10. The process of claim 1, wherein adduct is reduced using a reducing agent at a temperature of from about 20°

C. to about 250°

C.

11. The process of claim 1, wherein reacting glycerol with the metal catalyst to obtain hydroxyacetone occurs in a first reactor and wherein the hydroxyacetone is transferred to one or more other reactors to complete the reaction to the amino alcohol product.

12. The process of claim 11, wherein the first reactor is a trickle bed reactor.

13. The process of claim 1, wherein reducing the adduct using a reducing agent occurs in a trickle bed reactor.

14. The process of claim 1, wherein reacting glycerol with the metal catalyst occurs in a first trickle bed reactor and reducing the adduct using a reducing agent occurs in a second trickle bed reactor.

15. The process of claim 1, wherein reacting glycerol with the metal catalyst to obtain hydroxyacetone occurs in a first reactor and the hydroxyacetone is converted to the amino alcohol product in the first reactor.

16. The process of claim 15, wherein the first reactor is a trickle bed reactor.

17. The process of claim 1, wherein the glycerol is fed into a first reactor in one of a liquid phase and a gaseous phase.

18. A process for converting glycerol to an amino alcohol product comprising:

reacting glycerol with a metal catalyst at a temperature of from about 160°

C. to about 300°

C. to obtain hydroxyacetone;

reacting the hydroxyacetone with an amine compound at a temperature of from about −

20°

C. to about 150°

C. to obtain an adduct; and

reducing the adduct using a reducing agent at a temperature of from about 20°

C. to about 250°

C. to obtain an amino alcohol product.

19. The process of claim 18, wherein the metal catalyst is a catalyst selected from the group consisting of copper, chromium, nickel, zinc, cobalt, manganese, silicon, aluminum, copper chromite, copper zinc, oxides thereof, and combinations of any thereof.

20. The process of claim 18, the reducing agent comprises hydrogen in the presence of a hydrogenation catalyst selected from the group consisting of nickel, cobalt, RANEY®

nickel, RANEY®

cobalt, RANEY®

nickel or RANEY®

cobalt doped with other transition metals, nickel oxide, copper, palladium, platinum, rhodium, ruthenium, chromium, iridium, rhenium, manganese, molybdenum, iron, titanium, zirconium, magnesium, oxides thereof, and combinations of any thereof.

21. The process of claim 18, wherein the amine compound is a compound selected from the group consisting of ammonia, ammonium hydroxide, hydroxylamine, primary amines, secondary amine, alkanolamines and combinations of any thereof.

22. A process for converting glycerol to an amino alcohol having the formula:

23. The process of claim 22, wherein the metal catalyst is a catalyst selected from the group consisting of copper, chromium, nickel, zinc, cobalt, manganese, silicon, aluminum, copper chromite, copper zinc, oxides thereof and combinations of any thereof;

and

the reducing agent comprises hydrogen in the presence of a hydrogenation catalyst selected from the group consisting of nickel, cobalt, RANEY®

nickel, RANEY®

cobalt, RANEY®

nickel or RANEY®

cobalt doped with other transition metals, nickel oxide, copper, palladium, platinum, rhodium, ruthenium, chromium, iridium, rhenium, manganese, molybdenum, iron, titanium, zirconium, magnesium, oxides thereof, and combinations of any thereof.