IP Library Granted Patent US 7,790,932
Granted Patent B1
US 7,790,932 · App. 12/653,878 · Granted Sep 7, 2010

Hydroformylation process

Assignee: Lyondell Chemical Technology, L.P.
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 7,790,932
App. No.
12/653,878
Granted
Sep 7, 2010
Kind
B1
Abstract

A catalyst, useful for the hydroformylation of allyl alcohol, is described. The catalyst comprises a rhodium complex and a 6-bis(3,5-dialkylphenyl)phosphino-N-pivaloyl-2-aminopyridine or a 3-bis(3,5-dialkylphenyl)phosphino-2H-isoquinolin-1-one. The invention also includes a process for the production of 4-hydroxybutyraldehyde comprising reacting allyl alcohol with a mixture of carbon monoxide and hydrogen in the presence of a solvent and the catalyst. The process gives a high ratio of the linear product 4-hydroxybutyraldehyde to the branched co-product 3-hydroxy-2-methylpropionaldehyde.

Claims (14)

1. A process to produce 4-hydroxybutyraldehyde comprising reacting allyl alcohol with carbon monoxide and hydrogen in the presence of a solvent and a catalyst comprising a rhodium complex and a phosphine selected from the group consisting of a 6-bis(3,5-dialkylphenyl)phosphino-N-pivaloyl-2-aminopyridine and a 3-bis(3,5-dialkylphenyl)phosphino-2H-isoquinolin-1-one.

2. The process of claim 1 wherein the phosphine is 6-bis(3,5-dimethylphenyl)phosphino-N-pivaloyl-2-aminopyridine.

3. The process of claim 1 wherein the phosphine is 3-bis(3,5-dimethylphenyl)phosphino-2H-isoquinolin-1-one.

4. The process of claim 1 wherein the phosphine is a mixture of the 6-bis(3,5-dialkylphenyl)phosphino-N-pivaloyl-2-aminopyridine and a 3-diarylphosphino-2H-isoquinolin-1-one.

5. The process of claim 1 wherein the phosphine is a mixture of the 3-bis(3,5-dialkylphenyl)phosphino-2H-isoquinolin-1-one and a 6-diarylphosphino-N-pivaloyl-2-aminopyridine.

6. The process of claim 1 wherein the solvent is selected from the group consisting of C 5 -C 20 aliphatic hydrocarbons, C 6 -C 12 aromatic hydrocarbons, ethers, alcohols, and mixtures thereof.

7. The process of claim 1 wherein the solvent is selected from the group consisting of toluene, cyclohexane, methyl t-butyl ether, isopropanol, and mixtures thereof.

8. The process of claim 1 wherein the rhodium complex comprises rhodium and ligands selected from the group consisting of hydride, carbonyl, trialkyl phosphines, triaryl phosphines, diphosphines, cyclopentadienyls, 2,4-alkanedionates, and mixtures thereof.

9. The process of claim 1 further comprising hydrogenating the 4-hydroxybutyraldehyde in the presence of a hydrogenation catalyst to form 1,4-butanediol.

10. A catalyst comprising a rhodium complex and a phosphine selected from the group consisting of a 6-bis(3,5-dialkylphenyl)phosphino-N-pivaloyl-2-aminopyridine and a 3-bis(3,5-dialkylphenyl)phosphino-2H-isoquinolin-1-one.

11. The catalyst of claim 10 which comprises the rhodium complex and 6-bis(3,5-dimethylphenyl)phosphino-N-pivaloyl-2-aminopyridine.

12. The catalyst of claim 10 which comprises the rhodium complex and 3-bis(3,5-dimethylphenyl)phosphino-2H-isoquinolin-1-one.

13. The catalyst of claim 10 which comprises the rhodium complex and a mixture of the 6-bis(3,5-dialkylphenyl)phosphino-N-pivaloyl-2-aminopyridine and a 3-diarylphosphino-2H-isoquinolin-1-one.

14. The catalyst of claim 10 which comprises the rhodium complex and a mixture of the 3-bis(3,5-dialkylphenyl)phosphino-2H-isoquinolin-1-one and a 6-diarylphosphino-N-pivaloyl-2-aminopyridine.

Assignments (10)
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032123/0799 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: CITIBANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032125/0296 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032137/0156 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 23, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032137/0639 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: BANK OF AMERICA, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032138/0134 →
SECURITY AGREEMENT Recorded May 19, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0681 →
SECURITY AGREEMENT Recorded May 18, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0818 →
SECURITY AGREEMENT Recorded May 7, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024342/0801 →
SECURITY AGREEMENT Recorded May 6, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0421 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2010
From: WHITE, DANIEL F.; BOOGAERTS, INE; COLE-HAMILTON, DAVID JOHN
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 023902/0748 →