GB510936A - New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone - Google Patents

New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone

Info

Publication number
GB510936A
GB510936A GB35180/38A GB3518038A GB510936A GB 510936 A GB510936 A GB 510936A GB 35180/38 A GB35180/38 A GB 35180/38A GB 3518038 A GB3518038 A GB 3518038A GB 510936 A GB510936 A GB 510936A
Authority
GB
United Kingdom
Prior art keywords
give
tetrachloranthraquinone
tetraminoanthraquinone
toluenesulphonamide
dec
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
GB35180/38A
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.)
Rhodiaceta SA
Original Assignee
Rhodiaceta SA
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 Rhodiaceta SA filed Critical Rhodiaceta SA
Publication of GB510936A publication Critical patent/GB510936A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/22Dyes with unsubstituted amino groups

Landscapes

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

Abstract

510,936. Aminoanthraquinones. SOC. RHODIACETA. Dec. 2, 1938, No. 35180. Convention date, Dec. 24, 1937. [Class 2 (iii)] 1. 4. 5. 8 - Tetraminoanthraquinone is prepared by reacting 1.4.5.8-tetrachloranthraquinone with p-toluenesulphonamide and hydrolysing the condensation product thus obtained. In an example, anthraquinone is treated with chlorine in sulphuric acid containing a little iodine to give 1.4.5.8.-tetrachloranthraquinone, which is reacted with p-toluenesulphonamide in nitrobenzene in presence of copper powder, copper acetate and potassium carbonate to give a product which is hydrolysed by sulphuric acid to give the sulphate of 1.4.5.8-tetraminoanthraquinone. The free base may be dried in the pure state or mixed with a dispersing agent and dried.
GB35180/38A 1937-12-24 1938-12-02 New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone Expired GB510936A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR510936X 1937-12-24

Publications (1)

Publication Number Publication Date
GB510936A true GB510936A (en) 1939-08-10

Family

ID=8912076

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35180/38A Expired GB510936A (en) 1937-12-24 1938-12-02 New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone

Country Status (2)

Country Link
BE (1) BE510936A (en)
GB (1) GB510936A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2993074A (en) * 1958-02-10 1961-07-18 Hooker Chemical Corp Process for the production of phenols by decomposition of aralkyl hydroperoxides

Also Published As

Publication number Publication date
BE510936A (en) 1953-11-06

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