Preparation of derivatives of isobutene copolymers

Patent metadata

Field	Value
Publication number	US-9562117-B2
Application number	US-201113305132-A
Country	US
Kind code	B2
Filing date	Nov 28, 2011
Priority date	Nov 30, 2010
Publication date	Feb 7, 2017
Grant date	Feb 7, 2017

Abstract

A process for producing an isobutene copolymer derivative by: (I) free-radically copolymerizing (a) 10-90 mol % of a monoethylenically unsaturated C 4 - to C 12 -dicarboxylic acid, anhydride, or ester, (b) 10-90 mol % of a high-reactivity isobutene polymer having M n =110-250000 and obtained by polymerizing isobutene in the presence of an iron-halide-, aluminum trihalide-, or alkylaluminum halide-donor complex, each donor being an ether or carboxylic ester function, or in the presence of a Lewis acid complex containing an organic sulfonic acid, and (c) 0-50 mol % of a monoethylenically unsaturated compound copolymerizable with (a) and (b), to obtain an intermediate isobutene copolymer; and (II) reacting the carboxylic acid functions in the intermediate with at least one of ammonia, an amine, and an alcohol, to form a moiety containing at least one of a hydroxyl, carboxylic ester, amino, quaternized amino, amido, and imido group.

First claim

The invention claimed is:

1. A process for preparing an isobutene copolymer derivative, the process comprising:
(I) polymerizing isobutene monomers, or a monomer mixture comprising isobutene, in the presence of an aluminum trihalide-donor complex or an alkylaluminum halide-donor complex, and in the presence of an initiator, to form a high-reactivity isobutene homopolymer or copolymer having a number-average molecular weight (M n ) of 110 to 250000, a content of at least 50 mol % of terminal vinylidene double bonds per polyisobutene chain end, and comprising in reacted form a structural unit corresponding to the initiator,
wherein:
each complex comprises, as the donor, an organic compound comprising an ether or a carboxylic ester function;
a molar ratio of the donor to the aluminum trihalide, or of the donor to the alkylaluminum halide, in each complex is within a range from 0.3:1 to 1.5:1;
the initiator is selected from the group consisting of
an organic hydroxyl compound comprising two or more hydroxyl groups, or an organic hydroxyl compound having formula R 5 —OH, in which R 5 represents a C 6 - to C 20 -alkyl radical, a C 6 - to C 20 -aryl radical, or a mixture thereof;
an organic halogen compound comprising a halogen atom wherein each halogen atom is bound to an sp 3 -hybridized carbon atom; and
a protic acid,

a molar ratio of the initiator to the isobutene monomers, or to the monomer mixture, ranges from 0.0005:1 to 0.1:1; and
with a proviso that neither of a dihydrocarbyl ether nor 2-phenyl-2-propanol are present during the polymerizing, and with a proviso that the polymerizing (I) is not a living cationic polymerization;

(II) free-radically copolymerizing
(a) 10 to 90 mol % of at least one monoethylenically unsaturated C 4 - to C 12 -dicarboxylic acid or an anhydride, a monoester, or a diester of the dicarboxylic acid,
(b) 10 to 90 mol % of the high-reactivity isobutene homopolymer or copolymer, and
(c) 0 to 50 mol % of one or more monoethylenically unsaturated compound which is copolymerizable with components (a) and (b),

to obtain an intermediate isobutene copolymer; and then
(III) reacting at least a portion of the carboxylic acid, ester, or anhydride in the intermediate isobutene copolymer with at least one selected from the group consisting of
ammonia,
a monoamine or a polyamine of formula (IV):
HNR 13 R 14   (IV), and

an alcohol of formula (V):
R 15 OH  (V),

to form an isobutene copolymer derivative comprising at least one selected from the group consisting of a hydroxyl, a carboxylic ester, an amino, a quaternized amino, an amido, and an imido group,
wherein:
R 13 and R 14 are each independently a hydrogen, an aliphatic or aromatic hydrocarbyl radical, primary or secondary, an aromatic or an aliphatic aminoalkylene radical, a polyaminoalkylene radical, a hydroxylalkylene radical, a polyoxyalkylene radical optionally comprising an amino end group, or a heteroaryl or heterocyclyl radical optionally comprising an amino end group, or
R 13 and R 14 together with the nitrogen atom to which they are bonded form a ring, optionally comprising a further heteroatom; and
R 15 is independently an aliphatic radical, a cycloaliphatic radical, an aromatic hydrocarbyl radical, a hydroxyalkylene radical, or a polyoxyalkylene radical.

2. The process of claim 1 , wherein the polymerizing (I) carried out in the presence of an aluminum trichloride-donor complex.

3. The process of claim 1 , wherein the donor is a hydrocarbyl carboxylate of formula (III):
R 3 —COOR 4   (III),

wherein
R 3 and R 4 are each independently a C 1 - to C 20 -alkyl radical, a C 5 - to C 8 -cycloalkyl radical, a C 6 - to C 20 -aryl radical, or a C 7 - to C 20 -arylalkyl radical.

4. The process of claim 1 , wherein the donor has a total carbon number of 3 to 16.

5. The process of claim 1 , wherein the initiator is selected from the group consisting of:
an organic hydroxyl compound comprising two or more hydroxyl groups, or an organic hydroxyl compound having formula R 5 —OH, in which R 5 represents a C 6 - to C 20 -aryl radical, or a mixture thereof;
an organic halogen compound comprising a halogen atom, wherein each halogen atom is bound to an sp 3 -hybridized carbon atom; and
a protic acid.

6. The process of claim 5 , wherein the initiator is at least one selected from the group consisting of a protic acid, 1-phenyl ethanol, 1-(p-methoxy phenyl)ethanol 1-phenyl-1-chloroethane, 2-phenyl-2-chloropropane, tert-butyl chloride, 1,3-bis(1-hydroxy-1-methylethyl)benzene, and 1,4-bis(1-hydroxy-1-methylethyl)benzene.

7. The process of claim 1 , wherein the polymerizing (I) is carried out in the presence of 0.01 to 10 mmol of a nitrogen-comprising basic compound, based in each case on 1 mol of the isobutene monomer for a homopolymerization of isobutene or on 1 mol of a total amount of the polymerizable monomers for a copolymerization of isobutene.

8. The process of claim 7 , wherein the nitrogen-comprising basic compound is pyridine or a pyridine derivative.

9. The process of claim 1 , wherein the polymerizing (I) is carried out in the presence of at least one diluent selected from the group consisting of a halogenated aliphatic hydrocarbon, a halogen-free aliphatic hydrocarbon, an aromatic hydrocarbon and a mixture thereof.

10. The process of claim 1 , wherein the isobutene monomers are a technical C 4 hydrocarbon stream having an isobutene content of 1 to 100% by weight.

11. The process of claim 1 , wherein the polymerizing (I) comprises homopolymerizing isobutene or copolymerizing isobutene with up to 20% by weight of n-butene, to obtain a monofunctional high-reactivity isobutene polymer having a number-average molecular weight (M n ) of 500 to 5000.

12. The process of claim 1 , wherein the polymerizing (I) comprises homopolymerizing isobutene or copolymerizing isobutene with up to 20% by weight of n-butene in the presence of a difunctional or trifunctional initiator, to obtain a difunctional or trifunctional high-reactivity isobutene polymer having a number-average molecular weight (M n ) of 500 to 10 000.

13. The process of claim 1 , wherein the polymerizing (I) comprises copolymerizing isobutene with at least one vinylaromatic comonomer, and optionally with a difunctional or trifunctional initiator, to obtain a monofunctional, difunctional, or trifunctional component (b) having a number-average molecular weight (M n ) of 500 to 15000.

14. The process of claim 1 , wherein the monomer component (a) is maleic anhydride, fumaric acid, a fumaric monoester, or a fumaric diester.

15. The process of claim 1 , wherein copolymerization (II) occurs in the presence of the monomer of component (c) comprising at least one member selected from the group consisting of a monoethylenically unsaturated C 3 - to C 10 -monocarboxylic acid, an ester of the monoethylenically unsaturated C 3 - to C 10 -monocarboxylic acid, a linear 1-olefin having 2 to 40 carbon atoms, styrene, a styrene derivative, a vinyl ether having a total of 3 to 40 carbon atoms, and an allyl ether having a total of 4 to 41 carbon atoms.

16. The process of claim 1 , wherein:
the intermediate isobutene copolymer is reacted with the monoamine or polyamine of the formula (IV); and
any resulting carboxamide or carboximide derivative is optionally further reacted with at least one selected from the group consisting of a C 2 - to C 12 -dicarboxylic anhydride, a C 2 - to C 4 -alkylene carbonate, and boric acid.

17. The process of claim 1 , wherein the intermediate isobutene copolymer is reacte

Assignees

• König Hannah Maria
• Mühlbach Klaus
• Mach Helmut
• Eichenauer Ulrich
• Basf Se

Inventors

• König Hannah Maria
• Mühlbach Klaus
• Mach Helmut
• Eichenauer Ulrich

Classifications

• C08F8/32

  by reaction with amines · CPC title

• C08F8/42

  Introducing metal atoms or metal-containing groups · CPC title

• C08F290/042

  Polymers of hydrocarbons as defined in group C08F10/00 · CPC title

• C08F8/30 Primary

  Introducing nitrogen atoms or nitrogen-containing groups · CPC title

• C08F8/14

  Esterification · CPC title