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GB364141A - Improvements in and relating to the halogenation of anthraquinone and its derivatives - Google Patents

Improvements in and relating to the halogenation of anthraquinone and its derivatives

Info

Publication number
GB364141A
GB364141A GB2623030A GB2623030A GB364141A GB 364141 A GB364141 A GB 364141A GB 2623030 A GB2623030 A GB 2623030A GB 2623030 A GB2623030 A GB 2623030A GB 364141 A GB364141 A GB 364141A
Authority
GB
United Kingdom
Prior art keywords
derivatives
anthraquinone
halogenation
sunlight
positions
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
GB2623030A
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.)
ROBERT FRASER THOMSON
Imperial Chemical Industries Ltd
Original Assignee
ROBERT FRASER THOMSON
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 ROBERT FRASER THOMSON, Imperial Chemical Industries Ltd filed Critical ROBERT FRASER THOMSON
Priority to GB2623030A priority Critical patent/GB364141A/en
Publication of GB364141A publication Critical patent/GB364141A/en
Expired legal-status Critical Current

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

Abstract

Anthraquinones halogenated in the a -positions are obtained by halogenating anthraquinone and its halogen derivatives, capable of further halogenation in a -positions, in presence of sunlight or forms of light actinically active with or without halogen carriers and solvents or diluents. The products may be converted into amino, or substituted amino derivatives, including acylamino derivatives by known methods. An example is given of the halogenation of anthraquinone in oleum in presence of iodine and sunlight to 1 : 4 : 5 : 8-tetrachloranthraquinone, the product being treated with phthalimide followed by hydrolysis to convert it to the tetramino-derivative; this product dyes acetate silk in blue shades.
GB2623030A 1930-09-02 1930-09-02 Improvements in and relating to the halogenation of anthraquinone and its derivatives Expired GB364141A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2623030A GB364141A (en) 1930-09-02 1930-09-02 Improvements in and relating to the halogenation of anthraquinone and its derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2623030A GB364141A (en) 1930-09-02 1930-09-02 Improvements in and relating to the halogenation of anthraquinone and its derivatives

Publications (1)

Publication Number Publication Date
GB364141A true GB364141A (en) 1932-01-04

Family

ID=10240364

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2623030A Expired GB364141A (en) 1930-09-02 1930-09-02 Improvements in and relating to the halogenation of anthraquinone and its derivatives

Country Status (1)

Country Link
GB (1) GB364141A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1161252B (en) * 1962-03-22 1964-01-16 Bayer Ag Process for the preparation of 1, 4-dichloro-5-nitro-anthraquinone

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1161252B (en) * 1962-03-22 1964-01-16 Bayer Ag Process for the preparation of 1, 4-dichloro-5-nitro-anthraquinone

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