IP Library Granted Patent US 7,115,770
Granted Patent B2
US 7,115,770 · App. 10/398,837 · Granted Oct 3, 2006

Use of tin derivatives as catalysts

Assignee: Rhodia-Chimie
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Quick Facts
Patent No.
US 7,115,770
App. No.
10/398,837
Granted
Oct 3, 2006
Kind
B2
Abstract

The invention concerns the use as catalyst for transforming carbamates of compounds corresponding to the general formula (I): —Sn (X) (X′) wherein: X′ is selected among chloride, bromide, iodide, thiocyanate radicals, sulphonate radicals, advantageously perfluorinated on the carbon bearing the sulphonate function; X is selected among the values of X′ and among radicals of formula Y-Z; Y is selected among the chalcogen groups, advantageously light (that is oxygen and sulphur); Z is selected in the group consisting of trisubstituted tin, monosubstituted zinc, and the oxygenated acid radicals after ignoring the OH function. The invention is applicable to the coating industry.

Claims (30)

1. A transcarbamation process, comprising the step of reacting a carbamate vith an alcohol in the presence of an efficient catalytic amount, as transcarbamation catalyst, of compounds of general formula (I):

wherein:

X′ is chloride, bromide, iodide, thiocyanate radicals or sulfonate radicals;

X is X′ or radicals of formula Y-Z;

Y is a chalcogen; and

Z is trisubstituted tin, monosubstituted zinc or groups of oxygen-comprising acids, without the OH functional group.

2. The transcarbamation process according to claim 1 , wherein:

the X′ sulfonate radicals are perfluorinated on the carbon carrying the sulfonate functional group; and

Y is oxygen or sulfur.

3. The transcarbamation process according to claim 1 , wherein the catalyst is used in an amount of at least equal to 0.5% and at most equal to 5% as carbamate functional group equivalent.

4. The transcarbamation process according to claim 3 , wherein the amount is between 1% and 2%.

5. The transcarbamation process according to claim 1 , wherein X is X′.

6. The transearbamation process according to claim 1 , wherein one or more of the X or X′ groups are halides or thiocyanates.

7. The transcarbamation process according to claim 1 , wherein Z has the formula:

wherein X′ is as above defined.

8. The process according to claim 1 , wherein the transcarbamation reaction is carried out at a temperature of between 100 and 200° C.

9. The process according to claim 8 , wherein the temperature is between 120 and 180° C.

10. The process according to claim 1 , wherein X′ is a sulfonate radical perfluorinated on the carbon carrying the sulfonate functional group, and Y oxygen or sulfur.

11. A composition, comprising at least one carbamate capable of being obtained by reaction of a hydroxylated compound with an isocyanate and at least one compound of following general formula (I):

wherein:

X′ are sulfonate radicals:

X is X′ or radicals of formula Y-Z; and

Z is trisubstituted tin, monosubstituted zinc or groups of oxygen-comprising acids, without the OH functional group, wherein the isocyanate is aliphatic, the X′ sulfonate radicals are perfluorinated on the carbon carrying the sulfonate functional group; and

Y is oxygen or sulfur.

12. The composition according to claim 11 , further comprising an alcohol or polyalcohol.

13. The composition according to claim 12 , wherein the alcohol or polyalcohol is primary.

14. The composition according to claim 12 , wherein the hydroxylated compound is an alcohol volatile at a temperature at least equal to 150° C. or a hydroxylated masking agent.

15. The composition according to claim 14 , wherein the masking agent is a phenol or an oxime.

16. The composition according to claim 12 , wherein the hydroxylated compound is methanol.

17. The composition according to claim 11 , wherein wherein X′ is a sulfonate radical perfluorinated on the carbon carrying the sulfonate functional group, and Y oxygen or sulfur.

Assignments (3)
CHANGE OF NAME Recorded Oct 27, 2017
From: RHONE-POULENC CHIMIE
To: RHODIA CHIMIE
Reel/Frame 044309/0594 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2017
From: RHODIA CHIMIE
To: VENCOREX FRANCE
Reel/Frame 043970/0404 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2003
From: BERNARD, JEAN-MARIE; JOUSSEAUME, BERNARD; LAPORTE, CHRISTIAN; TOUPANCE, THIERRY
To: CHIMIE, RHODIA
Reel/Frame 014233/0122 →
Priority Claims (1)
FR 00 13164 · Oct 13, 2000 · national
Continuity (1)
Related Publication 20040087812A1 · May 6, 2004