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GB220302A - Manufacture of new intermediate products - Google Patents

Manufacture of new intermediate products

Info

Publication number
GB220302A
GB220302A GB18440/24A GB1844024A GB220302A GB 220302 A GB220302 A GB 220302A GB 18440/24 A GB18440/24 A GB 18440/24A GB 1844024 A GB1844024 A GB 1844024A GB 220302 A GB220302 A GB 220302A
Authority
GB
United Kingdom
Prior art keywords
naphthol
oxynaphthyl
triazine
cyanuric
chloride
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
GB18440/24A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB220302A publication Critical patent/GB220302A/en
Expired legal-status Critical Current

Links

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  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

p-Oxynaphthyl-1 : 3 : 5-triazine derivatives are produced by the action of a -naphthol upon a cyanuric halide having at least one replaceable halogen atom, in presence of a condensing agent such as aluminium chloride and in some cases with addition of a diluent such as carbon bisulphide, petroleum ether, tetrachlorethane or nitrobenzene. The cyanuric halide reacts with as many molecules of a -naphthol as it contains replaceable halogen atoms; the products have the general formula:- <FORM:0220302/2/1> where A and B are either further a -naphthol residues or any inorganic, aliphatic, or aromatic residues. The following examples are given:-(1) a mixture of cyanuric chloride and aluminium chloride is added to molten a -naphthol; the solid product forms an addition product with hydrochloric acid when boiled with a solution of that acid; it dissolves in caustic soda from which solution the 2 : 4 : 6-tri-p-oxynaphthyl-1 : 3 : 5-triazine, free from hydrochloric acid, is precipitated by a weak acid such as acetic acid or sodium bisulphite: (2) the same compound is prepared in presence of tetrachlorethane: (3) 2-phenylamino-4 : 6-di-p-oxynaphthyl-1 : 3 : 5-triazine is obtained from a -naphthol, aluminium chloride and the condensation product from equal molecules of cyanuric chloride and aniline: (4) 2 : 4-diamino-6-p-oxynaphthyl-1 : 3 : 5-triazine is prepared from chlorocyanuric diamide and a -naphthol, and 2 : 4-diphenylamino-6 - p-oxynaphthyl-1 : 3 : 5-triazine from a -naphthol and the condensation product from one molecular proportion of cyanuric chloride and two of aniline.
GB18440/24A 1923-08-09 1924-08-01 Manufacture of new intermediate products Expired GB220302A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH220302X 1923-08-09

Publications (1)

Publication Number Publication Date
GB220302A true GB220302A (en) 1925-01-15

Family

ID=4451593

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18440/24A Expired GB220302A (en) 1923-08-09 1924-08-01 Manufacture of new intermediate products

Country Status (1)

Country Link
GB (1) GB220302A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2133402A (en) * 1982-12-10 1984-07-25 Nippon Shinyaku Co Ltd Triazine derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2133402A (en) * 1982-12-10 1984-07-25 Nippon Shinyaku Co Ltd Triazine derivatives

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