GB203533A - Improvements in the manufacture and production of dyestuffs and intermediate products therefor - Google Patents

Improvements in the manufacture and production of dyestuffs and intermediate products therefor

Info

Publication number
GB203533A
GB203533A GB2536222A GB2536222A GB203533A GB 203533 A GB203533 A GB 203533A GB 2536222 A GB2536222 A GB 2536222A GB 2536222 A GB2536222 A GB 2536222A GB 203533 A GB203533 A GB 203533A
Authority
GB
United Kingdom
Prior art keywords
condensation product
sulphuric acid
dibenzanthrone
acid
condensing
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
GB2536222A
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Priority to GB2536222A priority Critical patent/GB203533A/en
Publication of GB203533A publication Critical patent/GB203533A/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
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/02Benzathrones
    • C09B3/06Preparation from starting materials already containing the benzanthrone nucleus

Landscapes

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

Abstract

Condensation products, which are probably 2 : 21-dibenzanthronyl compounds, are prepared by heating benzanthrone or its derivatives with alkaline condensing-agents under more moderate conditions than those yielding dibenzanthrone dyes; any dye simultaneously produced is removed by means of alkaline hydrosulphite. According to examples, benzanthrone is heated with caustic potash and ethyl or methyl alcohol, caustic potash in chlorbenzene, sodium anilide in aniline, or sodium methylanilide in methylaniline; the product forms yellow needles melting above 300 DEG C.; 6-methylbenzanthrone gives a similar product melting above 350 DEG C. These condensation products are converted into dibenzanthrone dyes by heating, with or without alkaline, acid, or oxidizing condensing-agents; if free halogens or sulphuric acid are used as condensing-agents the resulting dyes contain halogen or sulphonic groups; strongly oxidizing condensing-agents produce oxidized dibenzanthrones. According to examples:-dibenzanthrone is prepared by heating the benzanthrone condensation product described above with aluminium chloride in trichlorbenzene, mercuric sulphate and sulphuric acid, or caustic potash alone or in presence of a diluent; chlorinated dyes are obtained by heating the same condensation product with a mixture of ferric chloride and common salt, or ferric chloride in trichlorbenzene, or by dissolving the condensation product in chlorsulphonic acid and passing in chlorine. The same condensation product is boiled with sodium anilide in aniline, or other metal arylides may be used similarly; the same condensation product is treated with fuming sulphuric acid at a low temperature, and the resulting sulphonic acid is heated with mercuric sulphate and sulphuric acid giving a dibenzanthrone sulphonic acid; the condensation product is treated with manganese dioxide in sulphuric acid, giving an oxidized dibenzanthrone compound, which on reduction with bisulphite, gives a green dye; the sulphonated condensation product described above is treated with lead peroxide in sulphuric acid. Specifications 16538/04 and 14498/12 are referred to.
GB2536222A 1922-09-19 1922-09-19 Improvements in the manufacture and production of dyestuffs and intermediate products therefor Expired GB203533A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2536222A GB203533A (en) 1922-09-19 1922-09-19 Improvements in the manufacture and production of dyestuffs and intermediate products therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2536222A GB203533A (en) 1922-09-19 1922-09-19 Improvements in the manufacture and production of dyestuffs and intermediate products therefor

Publications (1)

Publication Number Publication Date
GB203533A true GB203533A (en) 1923-09-13

Family

ID=10226443

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2536222A Expired GB203533A (en) 1922-09-19 1922-09-19 Improvements in the manufacture and production of dyestuffs and intermediate products therefor

Country Status (1)

Country Link
GB (1) GB203533A (en)

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