GB487878A - Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series - Google Patents

Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series

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Publication number
GB487878A
GB487878A GB3575436A GB3575436A GB487878A GB 487878 A GB487878 A GB 487878A GB 3575436 A GB3575436 A GB 3575436A GB 3575436 A GB3575436 A GB 3575436A GB 487878 A GB487878 A GB 487878A
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GB
United Kingdom
Prior art keywords
amino
shades
artificial silk
silk
phosphorus
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
GB3575436A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB3575436A priority Critical patent/GB487878A/en
Publication of GB487878A publication Critical patent/GB487878A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Dyes are made by reacting anthraquinones or anthrapyrimidines having at least one primary amino group but no carboxylic or esterifiable hydroxy group with a phosphorus halide and treating the resulting compounds with aqueous alkaline agents. Amino compounds specified are 1-aminoanthraquinones, 1.4 - diaminoanthraquinones, 1.4.5.8 - tetraminoanthraquinones, 1 - amino - 4 - anilidoanthraquinones, 1 - amino - 4 - (p - aminophenyl)-aminoanthraquinones, aminoanthrapyrimidines, 1.4 - diamino - 2 - methoxyanthraquinone and 1.4 - diaminoanthraquinone - 2 - carboxylic acid amide. Phosphorus halides specified are phosphorus trichloride, pentachloride, oxychloride and the corresponding bromine and iodine compounds. Acid-binding agents which may be used are ammonia and organic bases such as pyridine, quinoline or dimethylaniline, which may also serve as solvents. The intermediate compounds, which contain halogen, may be converted to salts of phosphamic acids free from halogen by the use of aqueous alkaline agents such as caustic alkalies, or alkali carbonates. The products are soluble in water and dye acetate artificial silk, wool, silk, and viscose artificial silk fast shades. In examples: (1) 1.4 - diamino - 2 p - methoxyanthraquinone is reacted with phosphorus oxychloride, followed by treatment with sodium carbonate solution to give the sodium salt of the phosphamic acid; the free acid may be reconverted to the anthraquinone by heating with mineral acid and dyes acetate artificial silk, wool, or viscose artificial silk bluish-red shades; 1.4-diaminoanthraquinone (violet shades) or 1-amino-4-(p-aminophenyl)-aminoanthraquinone (blue shades) may also be used; (2) 1-amino-4-p-anisididoanthraquinone is reacted with phosphorus oxychloride, followed by treatment with caustic soda and sodium carbonate (blue shades); (3) phosphorus oxychloride is reacted with 1.4.5.8-tetraminoanthraquinone in pyridine, followed by treatment with caustic soda (blue shades on acetate artificial silk, wool, or silk); (4) phosphorus oxychloride is reacted with 4-amino-1.9-anthrapyrimidine in pyridine, followed by treatment with caustic soda (greenish-yellow shades on acetate artificial silk, wool or silk); (5) 1-aminoanthraquinone is reacted with phosphorus pentachloride in nitrobenzene, followed by treatment with caustic soda (yellow-red shades on acetate artificial silk).
GB3575436A 1936-12-30 1936-12-30 Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series Expired GB487878A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3575436A GB487878A (en) 1936-12-30 1936-12-30 Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3575436A GB487878A (en) 1936-12-30 1936-12-30 Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series

Publications (1)

Publication Number Publication Date
GB487878A true GB487878A (en) 1938-06-28

Family

ID=10381203

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3575436A Expired GB487878A (en) 1936-12-30 1936-12-30 Improvements in the manufacture and production of compounds of the anthraquinone and anthrapyrimidine series

Country Status (1)

Country Link
GB (1) GB487878A (en)

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