GB1378773A - Manufacture of anthraquinone compounds - Google Patents

Manufacture of anthraquinone compounds

Info

Publication number
GB1378773A
GB1378773A GB4719271A GB4719271A GB1378773A GB 1378773 A GB1378773 A GB 1378773A GB 4719271 A GB4719271 A GB 4719271A GB 4719271 A GB4719271 A GB 4719271A GB 1378773 A GB1378773 A GB 1378773A
Authority
GB
United Kingdom
Prior art keywords
compounds
boro
complex
anthraquinone
formula
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
GB4719271A
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.)
Imperial Chemical Industries Ltd
Original Assignee
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB4719271A priority Critical patent/GB1378773A/en
Publication of GB1378773A publication Critical patent/GB1378773A/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
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/503Amino-hydroxy-anthraquinones; Ethers and esters thereof unsubstituted amino-hydroxy anthraquinone
    • 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
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • 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
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/54Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
    • C09B1/545Anthraquinones with aliphatic, cycloaliphatic or araliphatic ether groups

Landscapes

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

Abstract

1378773 Preparation of anthraquinone compounds IMPERIAL CHEMICAL INDUSTRIES Ltd 11 Sept 1972 [11 Oct 1971] 47192/71 Heading C4P Anthraquinone compounds of the formula where X is OH or NH 2 , and R<SP>1</SP> and R<SP>2</SP> are H, Cl, Br, C 1 -C 4 alkyl or alkoxy, are prepared by subjecting a di-(boro-C 1 -C 4 alkyl carbonyloxy) complex of a compound of formula to the action of Cl 2 in oleum at -10-100‹ C. and thereafter hydrolysing off the boro-C 1 -C 4 alkylcarbonyloxy groups. The process may be carried out by passing Cl 2 through a solution of the said complex in oleum while stirring, and pouring the reaction mixture on to a mixture of ice and water to effect hydrolysis. A chlorination catalyst, such as iodine, may be present in the reaction medium. The compounds may be used as disperse dyes or as intermediates. The di-(boroalkylcarbonyloxy) complexes may be obtained by adding boric acid to the appropriate acid anhydride at 120‹ C., cooling and adding the anthraquinone compound, heating to 100‹ C. and cooling to 0‹ C. to isolate the complex. When chlorination takes place at below 30‹ C. then hydrolysis of the di-(boro-C 1 -C 4 alkylcarbonyloxy)-complexes gives compounds of the general formula
GB4719271A 1972-09-11 1972-09-11 Manufacture of anthraquinone compounds Expired GB1378773A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4719271A GB1378773A (en) 1972-09-11 1972-09-11 Manufacture of anthraquinone compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4719271A GB1378773A (en) 1972-09-11 1972-09-11 Manufacture of anthraquinone compounds

Publications (1)

Publication Number Publication Date
GB1378773A true GB1378773A (en) 1974-12-27

Family

ID=10444085

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4719271A Expired GB1378773A (en) 1972-09-11 1972-09-11 Manufacture of anthraquinone compounds

Country Status (1)

Country Link
GB (1) GB1378773A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4689078A (en) * 1985-09-02 1987-08-25 Canon Kabushiki Kaisha Recording liquid

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4689078A (en) * 1985-09-02 1987-08-25 Canon Kabushiki Kaisha Recording liquid

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Legal Events

Date Code Title Description
CSNS Application of which complete specification have been accepted and published, but patent is not sealed