GB1072956A - Esters of diisocyanato carboxylic acids and reaction products thereof - Google Patents
Esters of diisocyanato carboxylic acids and reaction products thereofInfo
- Publication number
- GB1072956A GB1072956A GB2320364A GB2320364A GB1072956A GB 1072956 A GB1072956 A GB 1072956A GB 2320364 A GB2320364 A GB 2320364A GB 2320364 A GB2320364 A GB 2320364A GB 1072956 A GB1072956 A GB 1072956A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- groups
- nco
- radical
- compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/771—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Emergency Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention comprises (a) compounds of the formula <FORM:1072956/C2/1> wherein each R1 is an alkoxyalkyl radical or halogenated alkoxyalkyl radical and R2 is a C1 to C8 alkylene or C1 to C8 alkylidene radical; (b) compounds of the formula <FORM:1072956/C2/2> wherein R1 and R2 are as defined above; and (c) reaction products of a compound of the formula <FORM:1072956/C2/3> wherein R1 is an unsubstituted or halogen-substituted alkyl, alkoxyalkyl, aryl, alkaryl, or aralkyl radical, R2 is as defined above, and R3 is a hydrogen atom or a radical <FORM:1072956/C2/4> with a polyol material sufficient in amount to provide a NCO/OH ratio of from 0.1 to 6.0, the reaction between the diisocyanate and the polyol taking place at a temperature and for a period of time sufficient to effect the reaction between NCO and OH groups and to minimize the reaction between NCO groups and active hydrogens present on groups other than the hydroxyl groups. The compounds of Formulae I, II and III may be prepared by reacting diamino compounds of the formula <FORM:1072956/C2/5> or acid-addition salts thereof, with phosgene in the presence of a solvent that will not react with phosgene under the reaction conditions employed. The polyol reactants from which products C above are obtained are defined in the Specification to be compounds, polymers or mixtures in which all species contain two or more hydroxyl groups per molecule and no other functional groups that react at a significant rate with an isocyanate group at 25 DEG C.ALSO:The invention comprises reaction products of a compound of formula <FORM:1072956/C3/1> wherein R1 is unsubstituted or halogen substituted alkyl, alkoxy-alkyl, aryl, alkaryl or aralkyl radical, R2 is a C1 to C8 alkylene or alkylidene radical, and R3 is a hydrogen atom or a radical <FORM:1072956/C3/2> , with a polyol meterial sufficient in amount to provide a NCO/OH ratio of from 0.1 to 6.0, the reaction between the diisocyanate and the polyol taking place at a temperature and for a period of time sufficient to effect the reaction between NCO and OH groups and to minimize the reaction between NCO groups and active hydrogen present on groups other than the hydroxyl groups. The polyol reactants are defined in the Specification to be compounds, polymers or mixtures in which all species contain two or more hydroxyl groups per molecule and no other functional groups that react at a significant rate with an isocyanate group at 25 DEG C. Adjuvants, e.g. antioxidants, pigments, plasticizers, catalysts and surfactants, may be included in the reaction mass. Those isocyanate-terminated reaction products prepared from reactants having an NCO/OH ratio greater than unit may be foamed to produce cellular materials or cured with amines or polyols to produce elastomeric compositions.ALSO:A metal plate is coated with the reaction product obtained by heating butanediol-1,4,trimethylol propane, and 2, 6-diisocyanato dimethyl pimelate in a mixture of methyl Cellosolve acetate (Cellosolve is a trade mark) and xylene at 80 DEG for 3 hours, adding phenol, cooling to room temperature and adding polypropylene glycol, and baking said coated surface at 400 DEG F in a circulating air oven (See Ex. 5). Wood and metal are coated with the reaction product obtained by heating 2, 5-diisocyanato n-decyl valerate and trimethylol propane at 70 DEG C for 3 hours, to which reaction product sufficient petroleum benzene has been added to give a solution of 65% solids and which has been pigmented with TiO2 (See Ex. 7).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7348360A | 1960-12-05 | 1960-12-05 | |
US285888A US3281378A (en) | 1963-06-06 | 1963-06-06 | Diisocyanato substituted aliphatic carboxylic acid ester urethane reaction products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1072956A true GB1072956A (en) | 1967-06-21 |
Family
ID=26754524
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4332261A Expired GB965474A (en) | 1960-12-05 | 1961-12-04 | Esters of di-isocyanate carboxylic acids |
GB534467A Expired GB1072958A (en) | 1960-12-05 | 1964-06-04 | Diaminocarboxylic acid esters |
GB2320364A Expired GB1072956A (en) | 1960-12-05 | 1964-06-04 | Esters of diisocyanato carboxylic acids and reaction products thereof |
GB681966A Expired GB1072957A (en) | 1960-12-05 | 1964-06-04 | Diaminocarboxylic acid esters |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4332261A Expired GB965474A (en) | 1960-12-05 | 1961-12-04 | Esters of di-isocyanate carboxylic acids |
GB534467A Expired GB1072958A (en) | 1960-12-05 | 1964-06-04 | Diaminocarboxylic acid esters |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB681966A Expired GB1072957A (en) | 1960-12-05 | 1964-06-04 | Diaminocarboxylic acid esters |
Country Status (5)
Country | Link |
---|---|
CH (2) | CH433253A (en) |
DE (2) | DE1418995A1 (en) |
GB (4) | GB965474A (en) |
NL (3) | NL6406398A (en) |
SE (1) | SE310422B (en) |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4469653A (en) * | 1981-07-04 | 1984-09-04 | Basf Aktiengesellschaft | Process for the preparation of molded parts of polyurethane or polyurethane-polyurea employing monocyclic amidines |
US5294445A (en) * | 1991-08-21 | 1994-03-15 | Bayer Aktiengesellschaft | Pesticidal shaped articles |
DE102007046187A1 (en) | 2007-09-26 | 2009-04-09 | Bayer Materialscience Ag | roof module |
WO2009142899A1 (en) | 2008-05-22 | 2009-11-26 | Dow Global Technologies Inc. | Thermoset polyurethanes comprising cis, trans-1, 3- and 1, 4-cyclohexanedimethylether groups |
EP2177555A2 (en) | 2008-10-16 | 2010-04-21 | Bayer MaterialScience AG | Method for manufacturing polyether ester polyols |
EP2202256A1 (en) | 2008-12-23 | 2010-06-30 | Bayer MaterialScience LLC | Polymer polyols comprising a natural oil base polyol, polyurethane foams comprising these polymer polyols and processes for their preparation |
WO2012084760A1 (en) | 2010-12-20 | 2012-06-28 | Bayer Materialscience Ag | Method for producing polyether ester polyols |
WO2013127850A1 (en) | 2012-02-29 | 2013-09-06 | Bayer Intellectual Property Gmbh | 2-k pultrusion formulation and process |
DE102012209598A1 (en) | 2012-06-06 | 2013-12-12 | Cht R. Beitlich Gmbh | Textile auxiliaries and thus refined textile product |
DE102012222045A1 (en) | 2012-12-03 | 2014-06-05 | Cht R. Beitlich Gmbh | Coating of luminophores |
EP2762508A1 (en) | 2007-07-23 | 2014-08-06 | Dow Global Technologies LLC | Two part polyurethane curable composition having substantially consistent G-modulus across the range of use temperatures |
WO2015100128A1 (en) | 2013-12-23 | 2015-07-02 | Dow Global Technologies Llc | Adhesive containing high solid copolymer polyol polyurethane prepolymer |
EP2894180A1 (en) | 2014-01-08 | 2015-07-15 | Bayer MaterialScience AG | Polymer Polyols comprising a Polyether Carbonate Polyol as the Base Polyol |
WO2017112012A2 (en) | 2015-09-17 | 2017-06-29 | Jerez Roberto Velozzi | Load-bearing composite panels, materials, products, and processes to make and use same |
WO2019149672A2 (en) | 2018-02-02 | 2019-08-08 | Basf Se | Simultaneous optimization of fiber sizing in-line with the pultrusion process |
EP3741788A1 (en) | 2019-05-24 | 2020-11-25 | Covestro Deutschland AG | Method for the preparation of polyoxyalkylenpolyol mixtures |
EP3838963A1 (en) | 2019-12-17 | 2021-06-23 | Covestro Deutschland AG | Method for producing polyoxyalkylene polyesterpolyols |
US11173224B2 (en) | 2017-07-21 | 2021-11-16 | The Procter & Gamble Company | Gels comprising a hydrophobic material |
WO2022060685A1 (en) | 2020-09-15 | 2022-03-24 | Dow Global Technologies Llc | Low odor polyurethane adhesives |
WO2022090358A1 (en) | 2020-10-28 | 2022-05-05 | Basf Se | Production of a polyester polyol with low voc emission |
WO2022096390A1 (en) | 2020-11-06 | 2022-05-12 | Covestro Deutschland Ag | Method for producing a polyol mixture |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3001013A1 (en) * | 1980-01-12 | 1981-07-23 | Basf Ag, 6700 Ludwigshafen | VINYLPYRROLIDONE POLYMERISATES, THEIR PRODUCTION AND THEIR USE FOR THE PRODUCTION OF BLOOD REPLACEMENT LIQUIDS |
US4749694A (en) * | 1984-04-26 | 1988-06-07 | Merck & Co., Inc. | Novel lysine esters used as absorption |
DE4334873A1 (en) * | 1993-10-13 | 1995-04-20 | Nycomed Arzneimittel Gmbh | Asymmetrically substituted diaminodicarboxylic acid derivatives and process for their preparation |
DE4417186A1 (en) * | 1994-05-17 | 1995-11-23 | Bayer Ag | New diisocyanates, a process for their preparation and their use |
EP3929177B1 (en) * | 2020-06-26 | 2023-11-29 | Evonik Operations GmbH | Method for the preparation of diisocyanates based on lysine |
CN118159578A (en) | 2021-10-07 | 2024-06-07 | 科思创德国股份有限公司 | Process for preparing polyoxyalkylene polyester polyols |
-
0
- NL NL133051D patent/NL133051C/xx active
- NL NL272185D patent/NL272185A/xx unknown
-
1961
- 1961-12-04 GB GB4332261A patent/GB965474A/en not_active Expired
- 1961-12-04 DE DE19611418995 patent/DE1418995A1/en active Pending
- 1961-12-05 CH CH1406661A patent/CH433253A/en unknown
-
1964
- 1964-04-21 SE SE494664A patent/SE310422B/xx unknown
- 1964-05-05 DE DE19641520384 patent/DE1520384B2/en not_active Withdrawn
- 1964-06-04 GB GB534467A patent/GB1072958A/en not_active Expired
- 1964-06-04 GB GB2320364A patent/GB1072956A/en not_active Expired
- 1964-06-04 GB GB681966A patent/GB1072957A/en not_active Expired
- 1964-06-05 CH CH738464A patent/CH471184A/en not_active IP Right Cessation
- 1964-06-05 NL NL6406398A patent/NL6406398A/xx unknown
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4469653A (en) * | 1981-07-04 | 1984-09-04 | Basf Aktiengesellschaft | Process for the preparation of molded parts of polyurethane or polyurethane-polyurea employing monocyclic amidines |
US5294445A (en) * | 1991-08-21 | 1994-03-15 | Bayer Aktiengesellschaft | Pesticidal shaped articles |
EP2762508A1 (en) | 2007-07-23 | 2014-08-06 | Dow Global Technologies LLC | Two part polyurethane curable composition having substantially consistent G-modulus across the range of use temperatures |
US8042864B2 (en) | 2007-09-26 | 2011-10-25 | Bayer Materialscience Ag | Roof module for a motor vehicle |
DE102007046187A1 (en) | 2007-09-26 | 2009-04-09 | Bayer Materialscience Ag | roof module |
WO2009142899A1 (en) | 2008-05-22 | 2009-11-26 | Dow Global Technologies Inc. | Thermoset polyurethanes comprising cis, trans-1, 3- and 1, 4-cyclohexanedimethylether groups |
EP2177555A2 (en) | 2008-10-16 | 2010-04-21 | Bayer MaterialScience AG | Method for manufacturing polyether ester polyols |
EP2202256A1 (en) | 2008-12-23 | 2010-06-30 | Bayer MaterialScience LLC | Polymer polyols comprising a natural oil base polyol, polyurethane foams comprising these polymer polyols and processes for their preparation |
WO2012084760A1 (en) | 2010-12-20 | 2012-06-28 | Bayer Materialscience Ag | Method for producing polyether ester polyols |
WO2013127850A1 (en) | 2012-02-29 | 2013-09-06 | Bayer Intellectual Property Gmbh | 2-k pultrusion formulation and process |
DE102012209598A1 (en) | 2012-06-06 | 2013-12-12 | Cht R. Beitlich Gmbh | Textile auxiliaries and thus refined textile product |
WO2013182568A2 (en) | 2012-06-06 | 2013-12-12 | Cht R. Beitlich Gmbh | Textile auxiliary agent and textile product finished therewith |
DE102012222045A1 (en) | 2012-12-03 | 2014-06-05 | Cht R. Beitlich Gmbh | Coating of luminophores |
WO2014086579A1 (en) | 2012-12-03 | 2014-06-12 | Cht R. Beitlich Gmbh | Luminophore coating |
WO2015100128A1 (en) | 2013-12-23 | 2015-07-02 | Dow Global Technologies Llc | Adhesive containing high solid copolymer polyol polyurethane prepolymer |
EP2894180A1 (en) | 2014-01-08 | 2015-07-15 | Bayer MaterialScience AG | Polymer Polyols comprising a Polyether Carbonate Polyol as the Base Polyol |
WO2017112012A2 (en) | 2015-09-17 | 2017-06-29 | Jerez Roberto Velozzi | Load-bearing composite panels, materials, products, and processes to make and use same |
EP3766686A1 (en) | 2015-09-17 | 2021-01-20 | Roberto Velozzi Jerez | Load-bearing composite panels, materials, products, and processes to make and use same |
US11173224B2 (en) | 2017-07-21 | 2021-11-16 | The Procter & Gamble Company | Gels comprising a hydrophobic material |
WO2019149672A2 (en) | 2018-02-02 | 2019-08-08 | Basf Se | Simultaneous optimization of fiber sizing in-line with the pultrusion process |
EP3741788A1 (en) | 2019-05-24 | 2020-11-25 | Covestro Deutschland AG | Method for the preparation of polyoxyalkylenpolyol mixtures |
WO2020239525A1 (en) | 2019-05-24 | 2020-12-03 | Covestro Intellectual Property Gmbh & Co. Kg | Process for producing polyoxyalkylene-polyol mixtures |
US12091543B2 (en) | 2019-05-24 | 2024-09-17 | Covestro Intellectual Property Gmbh & Co. Kg | Process for producing polyoxyalkylene-polyol mixtures |
EP3838963A1 (en) | 2019-12-17 | 2021-06-23 | Covestro Deutschland AG | Method for producing polyoxyalkylene polyesterpolyols |
WO2021122401A1 (en) | 2019-12-17 | 2021-06-24 | Covestro Intellectual Property Gmbh & Co. Kg | Process for preparing polyoxyalkylene polyester polyols |
WO2022060685A1 (en) | 2020-09-15 | 2022-03-24 | Dow Global Technologies Llc | Low odor polyurethane adhesives |
WO2022090358A1 (en) | 2020-10-28 | 2022-05-05 | Basf Se | Production of a polyester polyol with low voc emission |
WO2022096390A1 (en) | 2020-11-06 | 2022-05-12 | Covestro Deutschland Ag | Method for producing a polyol mixture |
Also Published As
Publication number | Publication date |
---|---|
NL272185A (en) | |
DE1418995A1 (en) | 1968-12-12 |
NL6406398A (en) | 1964-12-07 |
CH433253A (en) | 1967-04-15 |
SE310422B (en) | 1969-04-28 |
CH471184A (en) | 1969-04-15 |
GB1072957A (en) | 1967-06-21 |
DE1520384B2 (en) | 1972-04-20 |
NL133051C (en) | |
GB965474A (en) | 1964-07-29 |
DE1520384A1 (en) | 1969-03-20 |
GB1072958A (en) | 1967-06-21 |
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