IP Library Granted Patent US 8,710,278
Granted Patent B1
US 8,710,278 · App. 13/755,910 · Granted Apr 29, 2014

Process for producing polyols

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Quick Facts
Patent No.
US 8,710,278
App. No.
13/755,910
Granted
Apr 29, 2014
Kind
B1
Abstract

A process for producing polyols (such as neopentyl glycol) is disclosed which comprises reacting formaldehyde and another aldehyde in the presence of a trialkylamine catalyst and a base promoter to form an Aldol condensation reaction product. The base promoter improves removal of nitrogen containing salts prior to hydrogenation of the hydroxy aldehyde to produce the polyol. The improved process also reduces trialkylamine catalyst usage, improves trialkylamine catalyst recovery, and reduces nitrogen-containing salts prior to hydrogenation.

Claims (25)

1. A process for producing a polyol comprising:

contacting formaldehyde and another aldehyde in the presence of an amine catalyst and a promoter under Aldol condensation conditions to produce hydroxy aldehyde; and

hydrogenating the hydroxy aldehyde to form a polyol.

2. The process according to claim 1 , further comprising purifying said hydroxy aldehyde prior to hydrogenation and recovering said amine catalyst.

3. The process according to claim 1 , wherein the polyol is propylene glycol, ethylene glycol, dipropylene glycol, diethylene glycol, 1,4-butanediol, neopentyl glycol, triethanolamine, or glycerol.

4. The process according to claim 1 , wherein the hydroxy aldehyde is 3-hydroxypropanal, dimethylolethanal, trimethylolethanal (pentaerythrital), 3-hydroxybutanal (acetaldol), 3-hydroxy-2-ethylhexanal (butyl aldol), 3-hydroxy-2-methylpentanal (propyl aldol), 2-methylolpropanal, 2,2-dimethylolpropanal, 3-hydroxy-2-methylbutanal, 3-hydroxypentanal, 2-methylolbutanal, 2,2-dimethylolbutanal, or hydroxypivaldehyde.

5. The process according to claim 1 , wherein said another aldehyde is formaldehyde, propionaldehyde, n-butyraldehyde, isobutyraldehyde, valeraldehyde, 2-methylbutyraldehyde, 3-methylbutyraldehyde (isovaleraldehyde), 2,2-dimethylpropionaldehyde (pivalinaldehyde), caproaldehyde, 2-methylvaleraldehyde, 3-methylvaleraldehyde, 4-methylvaleraldehyde, 2-ethylbutyraldehyde, 2,2-dimethylbutyraldehyde, 3,3-dimethylbutyraldehyde, caprylic aldehyde, capric aldehyde, or glutaraldehyde.

6. The process according to claim 1 , wherein the amine catalyst is triethylamine, tri-n-propylamine, tri-n-butylamine, trimethlyamine, or mixtures thereof.

7. The process according to claim 1 , wherein the promoter is an alkali metal or alkaline earth metal of a carbonate, a hydrogen carbonate, a hydroxide, or mixtures thereof.

8. The process according to claim 7 , wherein the promoter is Na 2 CO 3 , K 2 CO 3 , CaCO 3 , NaHCO 3 , KHCO 3 , NaOH, KOH, Ca(OH) 2 , or combinations thereof.

9. A process for producing neopentyl glycol comprising:

contacting formaldehyde and isobutyraldehyde in the presence of an amine catalyst and a promoter under Aldol condensation conditions to produce hydroxypivaldehyde; and

hydrogenating the hydroxypivaldehyde to form neopentyl glycol.

10. The process according to claim 9 , further comprising purifying said hydroxypivaldehyde prior to hydrogenation and recovering said catalyst.

11. The process according to claim 9 , wherein the amine catalyst is triethylamine, tri-n-propylamine, tri-n-butylamine, trimethlyamine, or mixtures thereof.

12. The process according to claim 9 , wherein the promoter is an alkali metal or alkaline earth metal of a carbonate, a hydrogen carbonate, a hydroxide, or mixtures thereof.

13. The process according to claim 12 , wherein the promoter is Na 2 CO 3 , K 2 CO 3 , CaCO 3 , NaHCO 3 , KHCO 3 , NaOH, KOH, Ca(OH) 2 , or combinations thereof.

14. A process for producing a hydroxy aldehyde comprising:

contacting formaldehyde and another aldehyde in the presence of an amine catalyst and a promoter under Aldol condensation conditions to produce hydroxy aldehyde.

15. The process according to claim 14 , further comprising purifying said hydroxy aldehyde and recovering said catalyst.

16. The process according to claim 14 , wherein the hydroxy aldehyde is 3-hydroxypropanal, dimethylolethanal, trimethylolethanal (pentaerythrital), 3-hydroxybutanal (acetaldol), 3-hydroxy-2-ethylhexanal (butyl aldol), 3-hydroxy-2-methylpentanal (propyl aldol), 2-methylolpropanal, 2,2-dimethylolpropanal, 3-hydroxy-2-methylbutanal, 3-hydroxypentanal, 2-methylolbutanal, 2,2-dimethylolbutanal, or hydroxypivaldehyde.

17. The process according to claim 14 , wherein said another aldehyde is formaldehyde, propionaldehyde, n-butyraldehyde, isobutyraldehyde, valeraldehyde, 2-methylbutyraldehyde, 3-methylbutyraldehyde (isovaleraldehyde), 2,2-dimethylpropionaldehyde (pivalinaldehyde), caproaldehyde, 2-methylvaleraldehyde, 3-methylvaleraldehyde, 4-methylvaleraldehyde, 2-ethylbutyraldehyde, 2,2-dimethylbutyraldehyde, 3,3-dimethylbutyraldehyde, caprylic aldehyde, capric aldehyde, or glutaraldehyde.

18. The process according to claim 14 , wherein the amine catalyst is triethylamine, tri-n-propylamine, tri-n-butylamine, trimethlyamine, or mixtures thereof.

19. The process according to claim 14 , wherein the promoter is an alkali metal or alkaline earth metal of a carbonate, a hydrogen carbonate, a hydroxide, or mixtures thereof.

20. The process according to claim 19 , wherein the promoter is Na 2 CO 3 , K 2 CO 3 , CaCO 3 , NaHCO 3 , KHCO 3 , NaOH, KOH, Ca(OH) 2 , or combinations thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2013
From: HAMPTON, KENNETH WAYNE, JR.; BROWN, EUGENE H.; BROWN, THOMAS K.; PARIS, AMY K.; HOWE, KEVIN S.; PUCKETTE, THOMAS ALLEN
To: EASTMAN CHEMICAL COMPANY
Reel/Frame 031134/0968 →