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GB1116005A - Vinyl n-heterocyclic carbamates, process for their production and polymers thereof - Google Patents

Vinyl n-heterocyclic carbamates, process for their production and polymers thereof

Info

Publication number
GB1116005A
GB1116005A GB741166A GB741166A GB1116005A GB 1116005 A GB1116005 A GB 1116005A GB 741166 A GB741166 A GB 741166A GB 741166 A GB741166 A GB 741166A GB 1116005 A GB1116005 A GB 1116005A
Authority
GB
United Kingdom
Prior art keywords
vinyl
carbamates
heterocyclic
secondary amine
aziridinyl
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
GB741166A
Inventor
Lieng-Huang Lee
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Chemical Co filed Critical Dow Chemical Co
Priority to GB741166A priority Critical patent/GB1116005A/en
Publication of GB1116005A publication Critical patent/GB1116005A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F26/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
    • C08F26/06Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Vinyl N-heterocyclic carbamates of the general formula <FORM:1116005/C3/1> in which -A is the residue obtainable by removing the hydrogen atom from a secondary amine group in the ring of an N-heterocyclic secondary amine may be polymerized alone or in admixture with one or more ethylenically unsaturated monomers copolymerizable therewith, such as another vinyl N-heterocyclic carbamate, styrene, substituted styrenes, vinyl acetate or butyrate, vinylidene chloride, acrylic or methacrylic acid, ethyl acrylate, methyl methacrylate, acrylonitrile, N-isopropyl acrylamide, ethylene, propylene or 1-butene. Polymerization may be effected in bulk or in solution in benzene in the presence of a catalyst such a ,a 1-azobis-(isobutyronitrile), hydrogen or benzoyl peroxide or potassium persulphate. Examples describe the production of homopolymers of vinyl N-piperidinyl-, vinyl N-pyrrolyl- and vinyl N-aziridinyl carbamates. Vinyl N-aziridinyl carbamate is said to polymerize through both the aziridine ring and the vinyl group.ALSO:Compounds having the general formula <FORM:1116005/C2/1> in which -A is the residue obtainable by removing the hydrogen atom from a secondary amine group in the ring of an N-heterocyclic secondary amine, are prepared by reacting a vinylhaloformate with a compound of the general formula HA in which A is as above. Examples describe the production of vinyl N-piperidinyl, vinyl N-pyrrolyl and vinyl N-aziridinyl carbamates by reacting vinyl chloroformate with piperidine, pyrrole and ethyleneimine respectively. The carbamates of the invention can be employed as odoriferous ingredients in deodorizers or as herbicides.
GB741166A 1966-02-21 1966-02-21 Vinyl n-heterocyclic carbamates, process for their production and polymers thereof Expired GB1116005A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB741166A GB1116005A (en) 1966-02-21 1966-02-21 Vinyl n-heterocyclic carbamates, process for their production and polymers thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB741166A GB1116005A (en) 1966-02-21 1966-02-21 Vinyl n-heterocyclic carbamates, process for their production and polymers thereof

Publications (1)

Publication Number Publication Date
GB1116005A true GB1116005A (en) 1968-06-06

Family

ID=9832617

Family Applications (1)

Application Number Title Priority Date Filing Date
GB741166A Expired GB1116005A (en) 1966-02-21 1966-02-21 Vinyl n-heterocyclic carbamates, process for their production and polymers thereof

Country Status (1)

Country Link
GB (1) GB1116005A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3274681B2 (en) 1989-05-02 2002-04-15 ボーシュ アンド ローム インコーポレイティド New vinyl carbonate and vinyl carbamate contact lens material monomers
US8222200B2 (en) 2003-04-14 2012-07-17 Givaudan Sa Organic compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3274681B2 (en) 1989-05-02 2002-04-15 ボーシュ アンド ローム インコーポレイティド New vinyl carbonate and vinyl carbamate contact lens material monomers
US8222200B2 (en) 2003-04-14 2012-07-17 Givaudan Sa Organic compounds

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