GB1072956A - Esters of diisocyanato carboxylic acids and reaction products thereof - Google Patents

Esters of diisocyanato carboxylic acids and reaction products thereof

Info

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
Application number
GB2320364A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck and Co Inc
Original Assignee
Merck and Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US285888A external-priority patent/US3281378A/en
Application filed by Merck and Co Inc filed Critical Merck and Co Inc
Publication of GB1072956A publication Critical patent/GB1072956A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C265/00Derivatives of isocyanic acid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/771Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur oxygen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides 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)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (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).
GB2320364A 1960-12-05 1964-06-04 Esters of diisocyanato carboxylic acids and reaction products thereof Expired GB1072956A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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
WO2023057328A1 (en) 2021-10-07 2023-04-13 Covestro Deutschland Ag Process for preparing polyoxyalkylene polyester polyols

Cited By (27)

* Cited by examiner, † Cited by third party
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
DE102007046187A1 (en) 2007-09-26 2009-04-09 Bayer Materialscience Ag roof module
US8042864B2 (en) 2007-09-26 2011-10-25 Bayer Materialscience Ag Roof module for a motor vehicle
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
WO2014086579A1 (en) 2012-12-03 2014-06-12 Cht R. Beitlich Gmbh Luminophore coating
DE102012222045A1 (en) 2012-12-03 2014-06-05 Cht R. Beitlich Gmbh Coating of luminophores
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
EP3766686A1 (en) 2015-09-17 2021-01-20 Roberto Velozzi Jerez Load-bearing composite panels, materials, products, and processes to make and use same
WO2017112012A2 (en) 2015-09-17 2017-06-29 Jerez Roberto Velozzi 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
WO2020239525A1 (en) 2019-05-24 2020-12-03 Covestro Intellectual Property Gmbh & Co. Kg Process for producing polyoxyalkylene-polyol mixtures
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
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
DE1418995A1 (en) 1968-12-12
GB1072958A (en) 1967-06-21
NL6406398A (en) 1964-12-07
NL133051C (en)
GB1072957A (en) 1967-06-21
SE310422B (en) 1969-04-28
NL272185A (en)
DE1520384B2 (en) 1972-04-20
CH471184A (en) 1969-04-15
GB965474A (en) 1964-07-29
CH433253A (en) 1967-04-15
DE1520384A1 (en) 1969-03-20

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