α-olefin manufacturing process
View Patent ↗In an α-olefin manufacturing process by the oligomerization of ethylene using an iron complex of a diimine of a 2,6-diacylpyridine or a 2,6-pyridinecarboxaldehyde, in which certain substituted iminoaryl groups are present, less higher molecular weight unwanted products are produced when the diimine and/or its precursor arylamine does not have impurities with substitution on a second ortho position to the imino group. This leads to less fouling of the process apparatus and higher yields of desired α-olefins.
1. A process for the preparation of an improved symmetrical diimine of a 2,6-diacylpyridine or a 2,6-pyridinedicarboxaldehyde of the formula
wherein:
X 1 and X 2 are each independently carbon or nitrogen;
R 1 and R 2 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that when X 1 is nitrogen R 1 is not present, and when X 2 is nitrogen R 2 is not present;
R 3 is hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group;
R 4 and R 5 are each independently hydrogen, hydrocarbyl, or substituted hydrocarbyl;
R 6 and R 7 are the same, and are aryl groups in which a first ortho position is substituted by hydrocarbyl, substituted hydrocarbyl or a functional group, and a second ortho position is hydrogen or fluorine;
and provided that:
said symmetrical diimine of a 2,6-diacylpyridine or a 2,6-pyridinedicarboxaldehyde is made with a primary aromatic amine which contains no more than 0.5 mol percent of impurities which are themselves are primary aromatic amines and in which one of said second ortho positions is not hydrogen or fluorine;
and wherein said mol percent is based on the total amount of primary aromatic amines present.
2. The process as recited in claim 1 wherein X 1 and X 2 are carbon and R 1 , R 2 and R 3 are hydrogen.
3. The process as recited in claim 2 wherein said R 4 and R 5 are the same and are hydrogen or methyl.
4. The process as recited in claim 3 wherein R 6 and R 7 are
wherein:
R 8 is hydrocarbyl, substituted hydrocarbyl, or a functional group;
R 9 , R 10 , and R 11 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group; and
R 12 is hydrogen or fluorine.
5. The process as recited in claim 4 wherein R 8 is alkyl containing 1 to 4 carbon atoms, chloro, bromo, or alkoxy containing one to four carbon atoms.
6. The process as recited in claim 1 wherein said symmetrical diimine of a 2,6-diacylpyridine or a 2,6-pyridinedicarboxaldehyde is made with said primary aromatic amine which contains no more than 0.1 mol percent of impurities which are themselves primary aromatic amines and in which one of said second ortho positions is not hydrogen or fluorine.
7. The process as recited claim 6 wherein said primary aromatic amine is at least 99.5 mol percent of all primary aromatic amines present.
8. A symmetrical diimine of a 2,6-diacylpyridine or a 2,6-pyridinedicarboxaldehyde of the formula
wherein:
X 1 and X 2 are each independently carbon or nitrogen;
R 1 and R 2 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that when X 1 is nitrogen R 1 is not present, and when X 2 is nitrogen R 2 is not present;
R 3 is hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group;
R 4 and R 5 are each independently hydrogen, hydrocarbyl, or substituted hydrocarbyl;
R 6 and R 7 are the same, and are aryl groups in which a first ortho position is substituted by hydrocarbyl, substituted hydrocarbyl or a functional group, and a second ortho position is hydrogen or fluorine;
and provided that:
said symmetrical diimine of a 2,6-diacylpyridine or a 2,6-pyridinedicarboxaldehyde is made with a primary aromatic amine which contains no more than 0.5 mol percent of impurities which are themselves are primary aromatic amines and in which one of said second ortho positions is not hydrogen or fluorine;
and wherein said mol percent is based on the total amount of primary aromatic amines present.