IP Library Granted Patent US 9,133,083
Granted Patent B2
US 9,133,083 · App. 14/432,628 · Granted Sep 15, 2015

Continuous method for the production of neopentyl glycol

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,133,083
App. No.
14/432,628
Granted
Sep 15, 2015
Kind
B2
Abstract

A continuous method for preparing neopentyl glycol by addition of isobutyraldehyde and formaldehyde in the presence of a tertiary alkylamine as catalyst to give hydroxypivaldehyde with subsequent hydrogenation in the gas phase at a temperature of 125 to 180° C., is characterized in that the hydrogenation is carried out in the presence of a copper chromite catalyst comprising the activators barium and manganese and at a superatmospheric pressure of 30 to 120 kPa.

Claims (20)

1. Continuous method for preparing neopentyl glycol by addition of isobutyraldehyde and formaldehyde in the presence of a tertiary alkylamine as catalyst to give hydroxypivaldehyde with subsequent hydrogenation in the gas phase at a temperature of 125 to 180° C., characterized in that the hydrogenation is carried out in the presence of a copper chromite catalyst comprising the activators barium and manganese and at a superatmospheric pressure of 30 to 120 kPa.

2. Method according to claim 1 , characterized in that the hydrogenation is carried out in the presence of water in an amount of 15 to 25% by weight based on the total amount of the hydrogenation starting mixture used.

3. Method according to claim 1 , characterized in that the hydrogenation is carried out at a temperature of 140 to 180° C. and a superatmospheric pressure of 60 to 100 kPa.

4. Method according to claim 1 , characterized in that the tertiary alkylamines used are symmetrical tertiary alkylamines.

5. Method according to claim 4 , characterized in that the symmetrical tertiary alkylamines used are trimethylamine, triethylamine, tri-n-propylamine or tri-n-butylamine.

6. Method according to claim 1 , characterized in that the tertiary alkylamines used are asymmetrical tertiary alkylamines.

7. Method according to claim 1 , characterized in that the copper chromite catalyst comprises barium in an amount of 0.5 to 8% by weight and manganese in an amount of 0.5 to 8% by weight, in each case based on the total content of copper, chromium, barium and manganese.

8. Method according to claim 7 , characterized in that the copper chromite catalyst comprises barium in an amount of 1 to 4% by weight and manganese in an amount of 3 to 5% by weight, in each case based on the total content of copper, chromium, barium and manganese.

9. Method according to claim 1 , characterized in that the continuous gas phase hydrogenation is carried out in a cycle gas mode with a cycle gas stream and a fresh gas stream at a ratio of cycle gas stream to fresh gas stream of 40 to 70.

10. Copper chromite catalyst comprising barium in an amount of 0.5 to 0.8% by weight and manganese in an amount of 0.5 to 8% by weight, in each case based on the total content of copper, chromium, barium and manganese.

11. Method according to claim 1 , characterized in that the hydrogenation is carried out in the presence of water in an amount of 18 to 25% by weight, based on the total amount of the hydrogenation starting mixture used.

12. Method according to claim 2 , characterized in that the hydrogenation is carried out at a temperature of 140 to 180° C. and a superatmospheric pressure of 60 to 100 kPa.

13. Method according to claim 2 , characterized in that the tertiary alkylamines used are symmetrical tertiary alkylamines.

14. Method according to claim 3 , characterized in that the tertiary alkylamines used are symmetrical tertiary alkylamines.

15. Method according to claim 13 , characterized in that the symmetrical tertiary alkylamines used are trimethylamine, triethylamine, tri-n-propylamine or tri-n-butylamine.

16. Method according to claim 14 , characterized in that the symmetrical tertiary alkylamines used are trimethylamine, triethylamine, tri-n-propylamine or tri-n-butylamine.

17. Method according to claim 2 , characterized in that the tertiary alkylamines used are asymmetrical tertiary alkylamines.

18. Method according to claim 3 , characterized in that the tertiary alkylamines used are asymmetrical tertiary alkylamines.

19. Method according to claim 2 , characterized in that the copper chromite catalyst comprises barium in an amount of 0.5 to 8% by weight and manganese in an amount of 0.5 to 8% by weight, in each case based on the total content of copper, chromium, barium and manganese.

20. Method according to claim 3 , characterized in that the copper chromite catalyst comprises barium in an amount of 0.5 to 8% by weight and manganese in an amount of 0.5 to 8% by weight, in each case based on the total content of copper, chromium, barium and manganese.

Assignments (2)
CHANGE OF NAME Recorded Aug 25, 2021
From: OXEA GMBH
To: OQ CHEMICALS GMBH
Reel/Frame 057312/0979 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2015
From: EISENACHER, MATTHIAS; SCHALAPSKI, KURT; HEYMANNS, PETER; LUKAS, RAINER; STRUTZ, HEINZ
To: OXEA GMBH
Reel/Frame 035412/0628 →