GB220302A - Manufacture of new intermediate products - Google Patents
Manufacture of new intermediate productsInfo
- 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
Links
Landscapes
- 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.
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2133402A (en) * | 1982-12-10 | 1984-07-25 | Nippon Shinyaku Co Ltd | Triazine derivatives |
-
1924
- 1924-08-01 GB GB18440/24A patent/GB220302A/en not_active Expired
Cited By (1)
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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