GB731135A - Process for the production of reaction products of chlorotriazines - Google Patents

Process for the production of reaction products of chlorotriazines

Info

Publication number
GB731135A
GB731135A GB24990/53A GB2499053A GB731135A GB 731135 A GB731135 A GB 731135A GB 24990/53 A GB24990/53 A GB 24990/53A GB 2499053 A GB2499053 A GB 2499053A GB 731135 A GB731135 A GB 731135A
Authority
GB
United Kingdom
Prior art keywords
chloride
hydrogen
cyanuric chloride
chlorotriazines
triazine
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
GB24990/53A
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
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 Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Publication of GB731135A publication Critical patent/GB731135A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/24Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40Nitrogen atoms
    • C07D251/54Three nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40Nitrogen atoms
    • C07D251/54Three nitrogen atoms
    • C07D251/70Other substituted melamines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Substitution derivatives of triazine having a carbon-to-carbon bond are prepared by reacting a chlorotriazine, particularly cyanuric chloride, with benzene or a substituted benzene containing one or more alkyl groups, halogen atoms or other groups containing no labile hydrogen atom, e.g. a dimethylamino group, in the presence of hydrogen halide and a Friedel-Crafts catalyst. The reaction mixture is preferably saturated with hydrogen halide and 1 to 3 mols. of catalyst, e.g. aluminium chloride, are present per mol. of cyanuric chloride. The reaction may be controlled by the gradual addition of the aluminium chloride or cyanuric chloride with simultaneous super-saturation with hydrogen chloride. In examples (1) and (2), triphenyl-triazine is prepared from benzene and cyanuric chloride in the presence of hydrogen chloride and aluminium chloride; and (3) tri-chlorophenyl-triazine is prepared from chlorobenzene, cyanuric chloride, hydrogen chloride and aluminium chloride. In the last example, a mixture of ortho- and para-isomers is obtained and may be separated by extracting with hot tetrahydrofurane, the ortho-isomer being recovered from the filtrate and the para-isomer from the residue. The condensation of alkylbenzenes or dimethylaniline with cyanuric chloride also is referred to, as well as the use of other chlorotriazines such as mono-and di-chlorotriazines which are also substituted with alkyl, alkoxy or dimethylamino groups.
GB24990/53A 1952-10-11 1953-09-09 Process for the production of reaction products of chlorotriazines Expired GB731135A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE731135X 1952-10-11

Publications (1)

Publication Number Publication Date
GB731135A true GB731135A (en) 1955-06-01

Family

ID=6637639

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24990/53A Expired GB731135A (en) 1952-10-11 1953-09-09 Process for the production of reaction products of chlorotriazines

Country Status (1)

Country Link
GB (1) GB731135A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1169947B (en) * 1958-12-24 1964-05-14 Ciba Geigy Process for the preparation of 2- (2 ', 4'-dimethylphenyl) -4, 6-dichloro-1, 3, 5-triazine or 2, 4-di- (2', 4'-dimethylphenyl) -6-chloro- 1, 3, 5-triazine
CN108264490A (en) * 2016-12-30 2018-07-10 湖北尚赛光电材料有限公司 1,3,5- pyrrolotriazine derivatives and its preparation method and application

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1169947B (en) * 1958-12-24 1964-05-14 Ciba Geigy Process for the preparation of 2- (2 ', 4'-dimethylphenyl) -4, 6-dichloro-1, 3, 5-triazine or 2, 4-di- (2', 4'-dimethylphenyl) -6-chloro- 1, 3, 5-triazine
CN108264490A (en) * 2016-12-30 2018-07-10 湖北尚赛光电材料有限公司 1,3,5- pyrrolotriazine derivatives and its preparation method and application
CN108264490B (en) * 2016-12-30 2021-06-01 湖北尚赛光电材料有限公司 1,3, 5-triazine derivative and preparation method and application thereof

Similar Documents

Publication Publication Date Title
Thurston et al. Cyanuric chloride derivatives. I. Aminochloro-s-triazines
Dudley et al. Cyanuric chloride derivatives. III. Alkoxy-s-triazines
Cohen et al. The Effects of Structure on the Kinetics of Decomposition of Substituted Phenyl-azo-triphenylmethanes
GB1126804A (en) Triazine derivatives
GB731135A (en) Process for the production of reaction products of chlorotriazines
GB537690A (en) Process for the manufacture of derivatives of [1,3,5-triazinyl-(6)]-aminophenyl-arsonic acids
US2351333A (en) 6-(p-aminobenzene sulphonyl)-amino-2:4-dimethylpyrimidine and its manufacture
US2411670A (en) Halogen-b-htdeoxy-qtjinaldines
US1939025A (en) Aromatic amino-sulpho chlorides, substituted in the amino-group
GB1158700A (en) Adenosine Derivatives
GB1323094A (en) Production of triazine derivatives
ES394533A1 (en) 2-hydroxy-4-phenoxybenzophenone compounds
GB863547A (en) 3-mercapto-phenthiazine
US1923697A (en) Production of amino trimethylbenzenes
US2335273A (en) 3,3-dihalogenoxindoles
US1904229A (en) Gesellschaft
US2345215A (en) Manufacture of pyrimidine condensation products
US2777847A (en) Products
US2146899A (en) Compounds from aceto-halogen-sugars and nicotinic acid amide and process for the manufacture of same
US1817957A (en) 2.3 hydroxynaphthyl-arylketones
US2560824A (en) Method of preparing a triaryl
US1787315A (en) New compounds of the thiazolic series and process of making same
GB1258557A (en)
GB1254928A (en) beta-ALKOXYACRYLIC ACID AMIDES
ES237916A1 (en) Procedure for the preparation of new derivatives of the fenacine (Machine-translation by Google Translate, not legally binding)