GB943637A - Improvements in and relating to s-triazines - Google Patents

Improvements in and relating to s-triazines

Info

Publication number
GB943637A
GB943637A GB2895260A GB2895260A GB943637A GB 943637 A GB943637 A GB 943637A GB 2895260 A GB2895260 A GB 2895260A GB 2895260 A GB2895260 A GB 2895260A GB 943637 A GB943637 A GB 943637A
Authority
GB
United Kingdom
Prior art keywords
hydrocarbon
formula
compounds
unsubstituted
hydrogen
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
GB2895260A
Inventor
Richard Jonathon Hardy
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2895260A priority Critical patent/GB943637A/en
Publication of GB943637A publication Critical patent/GB943637A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
    • C08G73/0638—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with at least three nitrogen atoms in the ring
    • C08G73/0644—Poly(1,3,5)triazines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention comprises compounds of the formula: <FORM:0943637/C2/1> where R is an unsubstituted or substituted aryl group, e.g. phenoxy, naphthoxy, m-cresoxy or 2,4-dichlorophenoxy; and their production by reacting a compound of formula: <FORM:0943637/C2/2> with ammonia at temperatures up to 100 DEG C. Examples prepare the compound in which R is phenoxy; it is stated that above 100 DEG C. both phenoxy groups are replaced by amino groups. The first Provisional Specification refers to the production of compounds of the formula: <FORM:0943637/C2/3> where X1 is H, -C(R111)3, -NHR, -NR1R2 OH, -NHCOR or -NHSO2R (where R, R1 and R2 are hydrocarbon or fluorinated hydrocarbon groups and R111 is hydrogen, halogen or a hydrocarbon or fluorinated hydrocarbon group) and E1 is A2N-, -SH, -OR1 or -SR1 (where R1 is unsubstituted or substituted hydrocarbon) by reacting an amine A2NH with a compound: <FORM:0943637/C2/4> where E is -SH, -OR1 or -SR1; at least one A is preferably hydrogen. The second Provisional Specification relates to compounds of the formula: <FORM:0943637/C2/5> where R11 is hydrogen, halogen or a hydrocarbon or fluorinated hydrocarbon group, at least one R11 being halogen, A is hydrogen or a hydrocarbon or fluorinated hydrocarbon group, and E is -SH, -OR1 or -SR1, (where R1 is an unsubstituted or substituted hydrocarbon group; these compounds may be made by the process described in the first Provisional Specification. Neither Provisional Specification provides examples other than those given in the Complete Specification.ALSO:Compounds of the formula: <FORM:0943637/C3/1> where R is an unsubstituted or substituted aryl group (see Division C2) are said to form polymers by heating, to give a polymer with the repeating unit. <FORM:0943637/C3/2> It is also stated that 2,4-diphenoxy -6-trifluoro-methyl-s-triazin reacts with diamines to form polymers.
GB2895260A 1960-08-22 1960-08-22 Improvements in and relating to s-triazines Expired GB943637A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2895260A GB943637A (en) 1960-08-22 1960-08-22 Improvements in and relating to s-triazines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2895260A GB943637A (en) 1960-08-22 1960-08-22 Improvements in and relating to s-triazines

Publications (1)

Publication Number Publication Date
GB943637A true GB943637A (en) 1963-12-04

Family

ID=10283852

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2895260A Expired GB943637A (en) 1960-08-22 1960-08-22 Improvements in and relating to s-triazines

Country Status (1)

Country Link
GB (1) GB943637A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906751A (en) * 1987-11-19 1990-03-06 Ciba-Geigy Corporation Mercaptotriazine derivatives as lubricant additives
WO2016169831A1 (en) * 2015-04-24 2016-10-27 Basf Se Phenoxy- or pyridin-2-yloxy-aminotriazine compounds and their use as herbicides

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906751A (en) * 1987-11-19 1990-03-06 Ciba-Geigy Corporation Mercaptotriazine derivatives as lubricant additives
WO2016169831A1 (en) * 2015-04-24 2016-10-27 Basf Se Phenoxy- or pyridin-2-yloxy-aminotriazine compounds and their use as herbicides

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