SG11202108397WA - Phenyl isocyanate conversion process - Google Patents

Phenyl isocyanate conversion process

Info

Publication number
SG11202108397WA
SG11202108397WA SG11202108397WA SG11202108397WA SG11202108397WA SG 11202108397W A SG11202108397W A SG 11202108397WA SG 11202108397W A SG11202108397W A SG 11202108397WA SG 11202108397W A SG11202108397W A SG 11202108397WA SG 11202108397W A SG11202108397W A SG 11202108397WA
Authority
SG
Singapore
Prior art keywords
conversion process
phenyl isocyanate
isocyanate conversion
phenyl
isocyanate
Prior art date
Application number
SG11202108397WA
Inventor
Robert E Hefner
Helge Braun
Brian Cramm
Armenio Costa
Original Assignee
Dow Global Technologies Llc
Dow Portugal Produtos Quimicos Sociedade Unipessoal
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
Application filed by Dow Global Technologies Llc, Dow Portugal Produtos Quimicos Sociedade Unipessoal filed Critical Dow Global Technologies Llc
Publication of SG11202108397WA publication Critical patent/SG11202108397WA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C267/00Carbodiimides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C263/00Preparation of derivatives of isocyanic acid
    • C07C263/10Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene
    • 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
    • C08G18/02Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
    • C08G18/025Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing carbodiimide groups
    • 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
    • C08G18/721Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
    • C08G18/725Combination of polyisocyanates of C08G18/78 with other polyisocyanates
    • 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
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • 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
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • C08G18/7671Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
    • 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
    • C08G18/78Nitrogen
    • C08G18/79Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/797Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing carbodiimide and/or uretone-imine groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
SG11202108397WA 2019-02-07 2020-01-23 Phenyl isocyanate conversion process SG11202108397WA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201962802470P 2019-02-07 2019-02-07
PCT/US2020/014717 WO2020163092A1 (en) 2019-02-07 2020-01-23 Phenyl isocyanate conversion process

Publications (1)

Publication Number Publication Date
SG11202108397WA true SG11202108397WA (en) 2021-08-30

Family

ID=69726753

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202108397WA SG11202108397WA (en) 2019-02-07 2020-01-23 Phenyl isocyanate conversion process

Country Status (7)

Country Link
EP (1) EP3921349A1 (en)
JP (1) JP7498185B2 (en)
KR (1) KR20210126050A (en)
CN (1) CN113474388B (en)
BR (1) BR112021015332A2 (en)
SG (1) SG11202108397WA (en)
WO (1) WO2020163092A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114835609A (en) * 2021-02-01 2022-08-02 重庆恩联生物科技有限公司 Synthesis process of thermosensitive sensitizer N-p-toluenesulfonyl-N' - (3-p-toluenesulfonyloxyphenyl) urea

Family Cites Families (32)

* Cited by examiner, † Cited by third party
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US2663737A (en) 1951-08-07 1953-12-22 Du Pont Substituted phosphacyclopentene oxides and process of preparing them
US2663736A (en) 1951-08-07 1953-12-22 Du Pont Preparation of substituted phosphacyclopentene dihalides
US2663738A (en) 1951-08-07 1953-12-22 Du Pont Substituted phosphacyclopentene sulfides and process of preparing them
US2663739A (en) 1951-08-07 1953-12-22 Du Pont Substituted phosphacyclopentane oxides and process of preparing them
US3152131A (en) 1961-11-28 1964-10-06 Du Pont Catalyst for preparing carbodiimides
US4072712A (en) 1966-03-18 1978-02-07 Bayer Aktiengesellschaft Process for the production of carbodiimides and carbodiimide-isocyanate adducts
US3406198A (en) * 1966-08-05 1968-10-15 Upjohn Co Triarylarsines as catalysts for converting isocyanates to carbodiimides
US4118410A (en) 1971-02-04 1978-10-03 Gottfried Reuter Gmbh I.L. Polyphenyl-polymethylene-polyisocyanate mixtures
DE2504400A1 (en) * 1975-02-01 1976-08-05 Bayer Ag STORAGE-STABLE POLYISOCYANATE CONTAINING CARBODIIMIDE GROUPS
DE2504334A1 (en) * 1975-02-01 1976-08-05 Bayer Ag HIGH MOLECULAR, INSOLUBLE CARBODIIMIDIZATION CATALYSTS
GB1476088A (en) 1975-04-03 1977-06-10 Ici Ltd Carbodiimides
DE2552350A1 (en) * 1975-11-21 1977-05-26 Bayer Ag STORAGE-STABLE POLYISOCYANATE CONTAINING CARBODIIMIDE GROUPS
DE2552340A1 (en) * 1975-11-21 1977-06-02 Bayer Ag HIGH MOLECULAR, INSOLUBLE CARBODIIMIDIZATION CATALYSTS
DE2606419A1 (en) 1976-02-18 1977-08-25 Basf Ag STORAGE-STABLE, LIQUID POLYISOCYANATE CONTAINING CARBODIIMIDE GROUPS AND METHOD FOR THEIR MANUFACTURING
US4189354A (en) 1976-07-10 1980-02-19 Bayer Aktiengesellschaft Process for the production of diisocyanatodiphenyl methane isomers with an adjusted content of chlorine compounds
GB1567713A (en) 1977-01-31 1980-05-21 Upjohn Co Process for preparing carbodiimide-containing polyisocyanates
DE2837770C2 (en) 1978-08-30 1982-11-18 Basf Ag, 6700 Ludwigshafen Process for the preparation of storage-stable, liquid polyisocyanates containing carbodiimide groups
US4199524A (en) 1978-10-30 1980-04-22 Basf Wyandotte Corporation Stable liquid carbodiimide-containing polyisocyanate compositions
US4177205A (en) 1978-11-20 1979-12-04 Basf Wyandotte Corporation Process for the preparation of highly stable liquid carbodiimide-containing polyisocyanate compositions
DE2933601C2 (en) 1979-08-18 1985-07-11 Basf Ag, 6700 Ludwigshafen Process for obtaining mixtures of diphenyl methane diisocyanate isomers and optionally pure 4,4'-diphenyl methane diisocyanate with a low content of uretdiones and hydrolyzable chlorine compounds
DE3129270A1 (en) 1981-07-24 1983-02-10 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING POLYISOCYANATES
DE3413174A1 (en) 1984-04-07 1985-10-17 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING POLYISOCYANATES
US4743626A (en) 1987-09-14 1988-05-10 Basf Corporation Liquid carbodiimide-uretonimine modified polymethylene polyphenylene polyisocyanates and polyurethane foams made therefrom
DE19817691A1 (en) 1998-04-21 1999-10-28 Basf Ag Production of diphenylmethanediisocyanate and polyphenylene-polymethylene-polyisocynate mixtures
DE10245703A1 (en) * 2002-09-30 2004-04-01 Bayer Ag Process for the preparation of polyisocyanates of the diphenylmethane series by phosgenation of unneutralized polyamine of the diphenylmethane series
DE10333929A1 (en) * 2003-07-25 2005-02-24 Bayer Materialscience Ag Preparation of mixtures of di- and polyisocyanates of the diphenylmethane series with high contents of 4,4'-methylenediphenyl diisocyanate and 2,4'-methylenediphenyl diisocyanate
EP1773755B1 (en) 2004-07-28 2012-10-31 Huntsman International Llc Process for the production of polyisocyanates
US7504523B2 (en) * 2006-03-10 2009-03-17 Basf Corporation Uretonimine-modified isocyanate composition and method of forming the same
US7790907B2 (en) * 2006-07-21 2010-09-07 Basf Corporation Method of producing a uretonimine-modified isocyanate composition
FR2910706B1 (en) 2006-12-21 2009-03-20 Commissariat Energie Atomique INTERCONNECTION ELEMENT BASED ON CARBON NANOTUBES
KR102008545B1 (en) 2011-11-30 2019-08-07 다우 글로벌 테크놀로지스 엘엘씨 Process for the production of methylene diphenyl diisocyanate isomer mixtures with high 2,4'-methylene diphenyl diisocyanate purity
US11799707B2 (en) 2022-09-06 2023-10-24 Ultralogic 6G, Llc Guard-space phase-tracking reference signal for 5G and 6G networking

Also Published As

Publication number Publication date
US20220106264A1 (en) 2022-04-07
WO2020163092A1 (en) 2020-08-13
EP3921349A1 (en) 2021-12-15
KR20210126050A (en) 2021-10-19
JP2022519285A (en) 2022-03-22
CN113474388A (en) 2021-10-01
JP7498185B2 (en) 2024-06-11
BR112021015332A2 (en) 2021-10-05
CN113474388B (en) 2024-03-22

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