GB1119331A - New anthraquinone dyes - Google Patents

New anthraquinone dyes

Info

Publication number
GB1119331A
GB1119331A GB47379/65A GB4737965A GB1119331A GB 1119331 A GB1119331 A GB 1119331A GB 47379/65 A GB47379/65 A GB 47379/65A GB 4737965 A GB4737965 A GB 4737965A GB 1119331 A GB1119331 A GB 1119331A
Authority
GB
United Kingdom
Prior art keywords
alkyl
formula
oleum
hydroxyalkyl
halogen
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
GB47379/65A
Inventor
Willy Braun
Fritz Guellich
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
Publication of GB1119331A publication Critical patent/GB1119331A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/54—Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
    • C09B1/547—Anthraquinones with aromatic ether groups
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/56—Mercapto-anthraquinones
    • C09B1/58—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals
    • C09B1/585—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals substituted by aryl radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

The invention comprises anthraquinone dye-stuffs of the formula <FORM:1119331/C4-C5/1> wherein X represents H, alkyl or halogen; X1 represents H, alkyl or halogen; Y represents an O or S atom; A represents H or hydroxyalkyl and B represents H, alkyl or hydroxyalkyl. They may be obtained by reacting an anthraquinone compound of the formula <FORM:1119331/C4-C5/2> with chlorosulphonic acid, concentrated sulphuric acid or oleum in a molar ratio of 1:2, the sulphonic acid radicals being converted to sulphochloride radicals by treating with chlorinating agents in the case where sulphuric acid or oleum is used, and reacting the disulphochloride intermediate with a compound of the formula <FORM:1119331/C4-C5/3> in a molar ratio of 1:1 followed by hydrolysing the remaining sulphochloride group. Examples are given for the production of the compounds. They are useful for dyeing or printing fibrous material.
GB47379/65A 1964-11-10 1965-11-09 New anthraquinone dyes Expired GB1119331A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB79263A DE1283994B (en) 1964-11-10 1964-11-10 Process for making blue anthraquinone dyes

Publications (1)

Publication Number Publication Date
GB1119331A true GB1119331A (en) 1968-07-10

Family

ID=6980224

Family Applications (1)

Application Number Title Priority Date Filing Date
GB47379/65A Expired GB1119331A (en) 1964-11-10 1965-11-09 New anthraquinone dyes

Country Status (4)

Country Link
BE (1) BE672023A (en)
CH (1) CH469056A (en)
DE (1) DE1283994B (en)
GB (1) GB1119331A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1264242A (en) * 1959-07-24 1961-06-19 Geigy Ag J R New anthraquinone dyes and their preparation
FR1290522A (en) * 1960-05-12 1962-04-13 Basf Ag Dyes of the anthraquinonic series, containing sulfonic acid amide groups, and process for their production

Also Published As

Publication number Publication date
BE672023A (en) 1966-05-09
CH469056A (en) 1969-02-28
DE1283994B (en) 1968-11-28

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