GB331537A - Improvements in and relating to the production of anthraquinone derivatives - Google Patents

Improvements in and relating to the production of anthraquinone derivatives

Info

Publication number
GB331537A
GB331537A GB3832528A GB3832528A GB331537A GB 331537 A GB331537 A GB 331537A GB 3832528 A GB3832528 A GB 3832528A GB 3832528 A GB3832528 A GB 3832528A GB 331537 A GB331537 A GB 331537A
Authority
GB
United Kingdom
Prior art keywords
amino
chloranthraquinone
converted
anthraquinone
sulphoanthraquinone
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
GB3832528A
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.)
ERNEST GEORGE BECKETT
RHYS JENKIN LOVELUCK
Scottish Dyes Ltd
Original Assignee
ERNEST GEORGE BECKETT
RHYS JENKIN LOVELUCK
Scottish Dyes 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 ERNEST GEORGE BECKETT, RHYS JENKIN LOVELUCK, Scottish Dyes Ltd filed Critical ERNEST GEORGE BECKETT
Priority to GB3832528A priority Critical patent/GB331537A/en
Publication of GB331537A publication Critical patent/GB331537A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/24Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
    • C07C225/26Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings
    • C07C225/32Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings of condensed quinone ring systems formed by at least three rings
    • C07C225/34Amino anthraquinones

Landscapes

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

Abstract

331,537. Loveluck, R. J., Beckett, E. G., Thomas, J., and Scottish Dyes, Ltd. Dec. 28, 1928. Anthraquinone derivatives.-The products obtained by oxidizing an o-amino-#-sulphonic acid of anthraquinone with potassium persulphate in sulphuric acid are treated with a halogenating agent, for example sodium chlorate and hydrochloric acid, whereby the sulphonic acid group is replaced by halogen. Reduction of these halogenated derivatives by means of sodium hydrosulphide, or hydrogen sulphide and ammonia or neutral hydrosulphite yields the corresponding o-aminohalogen derivatives. By the persulphate oxidation 1-amino-2-sulpho-, and 2- amino-3-sulphoanthraquinone are converted to 1- nitroso-2-sulpho- and 2-nitro-3-sulpho-anthraquinone respectively, and the latter by the treatment with sodium chlorate and hydrochloric acid are converted to 1-nitroso-2-chlor- and 2-nitro-3- chloranthraquinone respectively. In example (1) 1-amino-2-sulphoanthraquinone is converted by the above processes to 1-nitroso-2-chloranthraquinone and the latter reduced with sodium hydrosulphide to 1-amino-2-chloranthraquinone; the product is purified by dissolving in strong sulphuric acid, diluting the solution when the sulphate precipitates out, filtering and decomposing the sulphate with water; (2) 2-amino-3- sulphoanthraquinone is converted by the above means to 2-nitro-3-chloranthraquinone and reduced with sodium hydrosulphide to 2-amino-3- chloranthraquinone. These products may also be purified as described in Specification 268,537.
GB3832528A 1928-12-28 1928-12-28 Improvements in and relating to the production of anthraquinone derivatives Expired GB331537A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3832528A GB331537A (en) 1928-12-28 1928-12-28 Improvements in and relating to the production of anthraquinone derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3832528A GB331537A (en) 1928-12-28 1928-12-28 Improvements in and relating to the production of anthraquinone derivatives

Publications (1)

Publication Number Publication Date
GB331537A true GB331537A (en) 1930-06-30

Family

ID=10402734

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3832528A Expired GB331537A (en) 1928-12-28 1928-12-28 Improvements in and relating to the production of anthraquinone derivatives

Country Status (1)

Country Link
GB (1) GB331537A (en)

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