USPatent applicationPatented

Process for the preparation of (cyclo)aliphatic uretdiones of improved color quality

Granted 23 Sep 2003 · 3 office actions

Current assignee: Evonik Degussa GmbH · originally Degussa Corporation

Law firm: Law firm · Log in to unlock

Attorney: Attorney · Log in to unlock

Inventors: Felix Schmitt, Elmar Wolf · Examiner: Deepak Rao · AU 1624 · TC 1600

Application· this page
8588087
filed 18 Jan 1996
Publication
Not published
not published
Patent
US 6,624,301
granted 23 Sep 2003

Life of the application

17 dated events
⤢ drag to zoom19961998200020022004200620082010201220142016ProsecutionOwnershipTerm & fees
ProsecutionOwnershipTerm & feeshover for detail · click to open

Abstract

Process for the preparation of (cyclo)aliphatic uretdiones of improved color quality by reaction of (cyclo)aliphatic diisocyanates, if desired in an inert solvent, with the aid of from 0.5 to 3% by weight of a catalyst of formula (I) in the presence of from 0.1 to 4% by weight of a phosphorus compound of formula (II)

Description

3 parts
›BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a process for the preparation of (cyclo)aliphatic uretdiones having improved color quality.

2. Discussion of the Background

The preparation of (cyclo)aliphatic uretdiones is described in DE-A 37 39 549. They can be processed to give lightfast PUR powders. A disadvantage of the (cyclo)aliphatic uretdiones of DE-A 37 39 549 is their more or less severe discoloration. Surprisingly, it has been possible to largely eliminate such discoloration if a trivalent, phosphorus compound is present during the dimerization of the diisocyanate.

›SUMMARY OF THE INVENTION

An object of the invention is to provide a process for the preparation of (cyclo)aliphatic uretdiones of improved color quality by reaction of (cyclo)aliphatic diisocyanates, if desired in an inert solvent, with the aid of from 0.5 to 3% by weight of a catalyst of formula (I)

in the presence of from 0.1 to 4% by weight of a phosphorus compound of formula (II)

›DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The invention provides a process for the preparation of (cyclo)aliphatic uretdiones of improved color quality by dimerization reaction of (cyclo)aliphatic diisocyanates, if desired in an inert solvent, with the aid of from 0.5 to 3% by weight of a catalyst of formula (I)

in which R 1 and R 2 are identical or different alkyl radicals of 1 to 8 carbon atoms or, together with the nitrogen atom to which they are attached, form a 5-membered or 6-membered ring which can contain a CH—CH 3 group, a N—CH 3 group or an oxygen atom in place of one CH 2 group in the ring,

in the presence of from 0.1 to 4% by weight of a phosphorus compound of formula (II)

in which R 3 and R 4 are identical or different aromatic or araliphatic hydrocarbon radicals of 1 to 10 carbon atoms or are OR 1 or OH. The dimerization is first carried out at temperatures of from 0 to 60° C. up to a conversion of from 5 to 70% and then the 1,3-diazacyclobutane-2,4-dione formed is isolated as a residue, without prior deactivation of the catalyst, from the reaction mixture by thin-film distillation. The amine catalyst, phosphorus compound and unreacted diisocyanate are isolated from the reaction mixture by thin-film distillation as the distillate. German patent application 195 10 956.2 filed Mar. 25, 1995 is incorporated herein by reference in its entirety.

The catalysts are employed in quantities of from 0.5 to 3% by weight, preferably from 1 to 2% by weight. They are N,N-disubstituted 4-aminopyridine derivatives, such as 4-dimethylaminopyridine, 4-diethylaminopyridine, 4-pyrrolidinopyridine, 4-piperidinopyridine and 4-(4-methylpiperidino)pyridine.

The phosphorus compounds are trivalent phosphorus compounds such as, for example, triphenylphosphine, triethyl phosphite, tributylphosphite, dibutylphosphite and dibenzylphosphite. They are added in quantities of from 0.1 to 4% by weight, preferably from 0.5 to 2% by weight, to the diisocyanate to be dimerized. The (cyclo)aliphatic diisocyanates employed according to the process of the invention contain from 6 to 15 carbon atoms.

The process according to the invention is conducted such that, first of all, dimerization is carried out with the aid of an amino catalyst and a phosphorus compound described above, up to a conversion degree which still permits conveying the reaction mixture in the liquid state at room temperature. This ranges generally from 20 to 60% diisocyanate conversion, preferably 30 to 50%. Then the unreacted diisocyanate together with the catalyst and the phosphorus compound are separated from the reaction product by thin-film distillation. The diisocyanate distilled off (plus catalyst and phosphorus compound) can be recycled to the reaction.

The reaction temperature is within a range from 0 to 60° C., preferably from 10 to 30° C. At higher temperatures, the catalytic conversion of the uretdione to the corresponding isocyanurate is clearly-evident.

The reaction time—the time within which, for example, from 40 to 60% of the diisocyanate has reacted—depends (at constant temperature) to a great extent on the concentration and on the nature of the catalyst employed. It is generally from 10 to 90 hours. The reaction can be carried out in polar solvents, such as esters, ethers and ketones, or without solvent. It is preferably carried out without solvent.

The reaction mixture is worked up by thin-film distillation at from 100 to 180° C. and from 0.01 to 0.5 mbar.

The uretdiones prepared by the process according to the invention are distinguished from the uretdiones of DE-A 37 39 549 by improved color quality.

EXAMPLES 1 TO 12

The uretdiones of isophorone diisocyanate (IPDI) listed in the table below were prepared by reacting, in a first stage, IPDI with the catalyst and with the phosphorus compound at 25° C. under N 2 blanketing up to a conversion of from 30 to 40% and, in a second step, separating off the unreacted IPDI together with the catalyst and phosphorus compound, by thin-film distillation at140° C./0.1 mbar, from the reaction product, which contained only slight traces of catalyst (0.05%) and phosphorus compound (<0.1%).

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.

›Tables in the description — 1
TABLE 1 — Catalytic dimerization of IPDI in the presence of triphenylphosphine
Example12345678
IPDI←----------------------------------------------------------------------→
DMAP*) % by wt.1212————
4-Pyrrolidinopyridine————1212
% by wt.
Triphenylphosphine——11——11
% by wt.
Reaction time hours7225722541184118
% NCO29.730.029.229.629.529.028.928.9
n D 251.49321.49251.49421.49401.49291.49401.49481.4956
Color (Hazen)267389114112303361130183
↓ Thin-film distillation 140° C./0.1 mbar
% NCO17.617.917.817.817.517.617.417.8
% IPDI0.60.70.60.30.30.50.30.3
Color number (Hazen)248227147219308401250223
(70% strength in butyl
acetate)
*)4-Dimethylaminopyridine

Claims as granted

15 claims

Log in to read the claims of this application.

Log in to unlock

Classifications

5 codes
IPC · International Patent Classification
Section C — Chemistry; metallurgy
  • C08G18/79
  • C07D229/00
  • C08G18/02
  • C08K5/50
USPC · US Patent Classification
540/202

Claim changes

Soon
Coming soonHow the claims changed between publication and grant

See which claims were amended, added or cancelled during examination, with every added and removed word marked.

AmendedAddedCancelledUnchanged

The published claims of this application are not paired with the granted ones in what we hold.

File wrapper

⤢ drag to zoom199619971998199920002001200220032004USPTOApplicantNon-final rejectionFinal rejectionNon-final rejection
USPTOApplicanthover for detail · click to open
Pendency
7.7 y
2,805 days filing → grant
Office actions
3
non-final + final
Responses
2
no RCE
Interviews
1
examiner interview summaries
Examiner
Deepak Rao
art unit 1624 · TC 1600
Citations: 7 back · 1 forward

See the full prosecution history — every USPTO and applicant action on this file, in order.

Log in to unlock

Documents

Log in to open the documents of this file: the application as filed, every office action and response, the notice of allowance.

Log in to unlock

Chain of title

⤢ drag to zoom19961998200020022004200620082010201220142016Owner 2Owner 4Owner 7
Titlehover for detail · click to open

See the full assignment history — every owner this patent has passed through, with recordation dates and reel/frame numbers.

Log in to unlock