IP Library Granted Patent US 10,544,174
Granted Patent B2
US 10,544,174 · App. 15/649,743 · Granted Jan 28, 2020

Process for the alkoxycarbonylation of ethylenically unsaturated compounds with monophosphine ligands

Inventors: Kaiwu Dong (Bo Zhou, CN); Ralph Jackstell (Cuxhaven Altenwalde, DE); Matthias Beller (Ostseebad Nienhagen, DE); Dirk Fridag (Haltern am See, DE); Dieter Hess (Marl, DE); Katrin Marie Dyballa (Recklinghausen, DE); Frank Geilen (Haltern am See, DE); Robert Franke (Marl, DE)
Assignee: EVONIK DEGUSSA GMBH
C07F9/5045C07C67/38C07F15/0066C07D403/14C07D405/14
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 10,544,174
App. No.
15/649,743
Granted
Jan 28, 2020
Kind
B2
Abstract

The invention relates to a process comprising the following process steps: a) introducing an ethylenically unsaturated compound; b) adding a monophosphine ligand and a compound which comprises Pd, or adding a complex comprising Pd and a monophosphine ligand; c) adding an aliphatic alcohol; d) supplying CO; e) heating the reaction mixture, the ethylenically unsaturated compound being reacted to form an ester; where the monophosphine ligand is a compound of formula (I) where R 1 is selected from —(C 1 -C 12 )-alkyl, —O—(C 1 -C 12 )-alkyl, —O—(C 6 -C 20 )-aryl, —(C 6 -C 20 )-aryl, —(C 3 -C 12 )-cycloalkyl, —(C 3 -C 12 )-heterocycloalkyl, —(C 3 -C 20 )-heteroaryl; R 2 is selected from —(C 6 -C 20 )-aryl, —(C 3 -C 12 )-cycloalkyl, —(C 3 -C 12 )-heterocycloalkyl, —(C 3 -C 20 )-heteroaryl; R 3 is —(C 3 -C 20 )-heteroaryl; and R 1 , R 2 and R 3 may each independently be substituted by one or more substituents selected from —(C 1 -C 12 )-alkyl, —(C 3 -C 12 )-cycloalkyl, —(C 3 -C 12 )-heterocycloalkyl, —O—(C 1 -C 12 )-alkyl, —O—(C 1 -C 12 )-alkyl-(C 6 -C 20 )-aryl, —O—(C 3 -C 12 )-cycloalkyl, —S—(C 1 -C 12 )-alkyl, —S—(C 3 -C 12 )-cycloalkyl, —COO—(C 1 -C 12 )-alkyl, —COO—(C 3 -C 12 )-cycloalkyl, —CONH—(C 1 -C 12 )-alkyl, —CONH—(C 3 -C 12 )-cycloalkyl, —CO—(C 1 -C 12 )-alkyl, —CO—(C 3 -C 12 )-cycloalkyl, —N—[(C 1 -C 12 )-alkyl] 2 , —(C 6 -C 20 )-aryl, —(C 6 -C 20 )-aryl-(C 1 -C 12 )-alkyl, —(C 6 -C 20 )-aryl-O—(C 1 -C 12 )-alkyl, —(C 3 -C 20 )-heteroaryl, —(C 3 -C 20 )-heteroaryl-(C 1 -C 12 )-alkyl, —(C 3 -C 20 )-heteroaryl-O—(C 1 -C 12 )-alkyl, —COOH, —OH, —SO 3 H, —NH 2 , halogen.

Claims (10)

1. A regioselective process for preparing an ester comprising the following process steps:

a) introducing an ethylenieally unsaturated compound having 8 to 12 carbon atoms, forming a reaction mixture;

b) adding a monophosphine ligand and a compound which comprises Pd, or adding a complex comprising Pd and a monophosphine ligand;

c) adding an aliphatic alcohol;

d) supplying CO;

e) heating the reaction mixture, the ethylenically unsaturated compound being reacted with the epithelium CO and aliphatic alcohol to form the ester; where the monophosphine ligand is

2. The process according to claim 1 , wherein the ethylenically unsaturated compound is selected from the group consisting of ethene, propene, 1-butene, 2-butene, isobutene, 1,3-butadiene, 1-pentene, 2-pentene, 2-methyl-1-butene, 3-methyl-1-butene, 2-methyl-2-butene, hexene, tetramethylethylene, heptene, 1-octene, 2-octene, di-n-butene, and mixtures thereof.

3. The process according to claim 1 , wherein the compound comprising Pd in process step b) is selected from the group consisting of palladium dichloride, palladium(II) acetylacetonate, palladium(II) acetate, dichloro(1,5-cyclooctadiene)palladium(II), bis(dibenzylideneacetone)palladium, bis(acetonitrile)dichloro-palladium(II), and palladium(cinnamyl) dichloride.

4. The process according to claim 1 , wherein the alcohol in process step c) is selected from the group consisting of methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol, 2-propanol, tert-butanol, 3-pentanol, cyclohexanol, and mixtures thereof.

5. The process according to claim 1 , wherein the alcohol in process step c) is selected from the group consisting of methanol and ethanol.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2024
From: EVONIK OPERATIONS GMBH
To: EVONIK OXENO GMBH & CO. KG
Reel/Frame 066242/0585 →
CHANGE OF NAME Recorded Mar 29, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 052254/0052 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2018
From: DONG, KAIWU; JACKSTELL, RALF; BELLER, MATTHIAS; FRIDAG, DIRK; HESS, DIETER; DYBALLA, KATRIN MARIE; GEILEN, FRANK; FRANKE, ROBERT
To: EVONIK DEGUSSA GMBH
Reel/Frame 045302/0896 →
Priority Claims (1)
EP 16180050 · Jul 19, 2016 · regional
Continuity (1)
Related Publication 20180022764A1 · Jan 25, 2018