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US5498747A Expired / Lapsed US ⏱️ 0.0 years remaining

Carbodiimides and/or oligomeric polycarbodiimides based on 1,3-bis (1-methyl-1-isocyanatoethyl)benzene, their preparation, and their use as hydrolysis stabilizers

Assignee: BASF SE
•
Filing: 1995-03-07
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Granted: 1996-03-12
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Expires: 2015-03-07
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Abstract

Abstract The present invention relates to novel carbodiimides or oligomeric polycarbodiimides containing terminal isocyanate, urea and/or urethane groups, methods for their preparation, and their use as hydrolysis stabilizers.

Inventors

  • 👤 Siegmund Pohl
  • 👤 Friedhelm Lehrich
  • 👤 Manfred Genz
  • 👤 Bernd Bruchmann
  • 👤 Helmut Tesch
  • 👤 Roland Minges
  • 👤 Joachim Streu

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 13:26
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/2805; C08G18/2815; C08G18/283; C07; C07C; C07C267/00; C07C273/00; C07C273/18; C07C273/1809; C07C273/1818; C07C273/1827; C08G18/282; C08G18/2825; C08G18/285; C08G18/2865; C08G18/65; C08G18/66; C08G18/6633; C08G18/6637; C08G18/664; C08G18/70; C08G18/72; C08G18/77; C08G18/78; C08G18/79; C08G18/797; C08L; C08L75/00; C08L75/04

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 182 words
A process for the preparation of a carbodiimide or oligomeric polycarbodiimide of the formula; ##STR4## where the R radicals are identical or different and are selected from the group consisting of --NCONHR 1 , --NHCONR 1 R 2 --, and --NHCOOR 3 --, where R 1 and R 2 may be identical or different and are alkyl, cycloalkyl, or aralkyl, and R 3 is identical to R 1 or is alkoxypolyoxyalkylene, and n is an integer from 0 to 10, which comprises a) condensing 1,3-bis(1-methylisocyanatoethyl)benzene in the presence of catalysts with elimination of carbon dioxide, subsequently reacting all or some of the free terminal isocyanate groups of the resultant (poly)carbodiimide with at least one aliphatic, cycloaliphatic or araliphatic amine, alcohol and/or alkoxypolyoxyalkylene alcohol, and then removing or deactivating the catalysts, or b) reacting up to 50% of the isocyanate groups of 1,3-bis(1-methyl-1-isocyanatoethyl)benzene with at least one aliphatic, cycloaliphatic or araliphatic amine, alcohol and/or alkoxypolyoxyalkylene alcohol, subsequently condensing all or some of the free isocyanate groups in the presence of catalyst with elimination of carbon dioxide, and then removing or deactivating the catalysts.
Claim 2
Dependent Claim 182 words
A process for the preparation of a carbodiimide or oligomeric polycarbodiimide of the formula; ##STR4## where the R radicals are identical or different and are selected from the group consisting of --NCONHR 1 , --NHCONR 1 R 2 --, and --NHCOOR 3 --, where R 1 and R 2 may be identical or different and are alkyl, cycloalkyl, or aralkyl, and R 3 is identical to R 1 or is alkoxypolyoxyalkylene, and n is an integer from 0 to 10, which comprises a) condensing 1,3-bis(1-methylisocyanatoethyl)benzene in the presence of catalysts with elimination of carbon dioxide, subsequently reacting all or some of the free terminal isocyanate groups of the resultant (poly)carbodiimide with at least one aliphatic, cycloaliphatic or araliphatic amine, alcohol and/or alkoxypolyoxyalkylene alcohol, and then removing or deactivating the catalysts, or b) reacting up to 50% of the isocyanate groups of 1,3-bis(1-methyl-1-isocyanatoethyl)benzene with at least one aliphatic, cycloaliphatic or araliphatic amine, alcohol and/or alkoxypolyoxyalkylene alcohol, subsequently condensing all or some of the free isocyanate groups in the presence of catalyst with elimination of carbon dioxide, and then removing or deactivating the catalysts.
Claim 3
Dependent Claim 54 words
The process of claim 1, which comprises condensing 1,3-bis(1-methyl-1-isocyanatoethyl)-benzene in the presence of catalyst with elimination of carbon dioxide, subsequently reacting all or some of the free terminal isocyanate groups of the resultant (poly)carbodiimide with at least one aliphatic, cycloaliphatic or araliphatic amine, alcohol and/or alkoxypolyoxyalkylene alcohol, and then removing or deactivating the catalysts.
Claim 4
Dependent Claim 33 words
The process as claimed in claim 1, wherein the catalyst used for the condensation is at least one phosphorus compound selected from the group consisting of phospholenes, phospholene oxides, phospholidines and phospholidine oxides.
Claim 5
Dependent Claim 33 words
The process as claimed in claim 2, wherein the catalyst used for the condensation is at least one phosphorus compound selected from the group consisting of phospholenes, phospholene oxides, phospholidines and phospholidine oxides.

References Cited (Backward Citations)

DE113059C Cited
GB851936A Cited
US2941983A Cited
US3193522A Cited
US3193523A Cited
US4419294A Cited
US5008363A Cited
EP0460481A2 Cited
US5210170A Cited
US5246993A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1999-03-12 1999-09-11 2000-03-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2003-03-12 2003-09-11 2004-03-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2007-03-12 2007-09-11 2008-03-12 $7700.00 Window Closed / Lapsed

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