GB633486A - Manufacture of new dyestuffs of the anthraquinone series - Google Patents

Manufacture of new dyestuffs of the anthraquinone series

Info

Publication number
GB633486A
GB633486A GB3488646A GB3488646A GB633486A GB 633486 A GB633486 A GB 633486A GB 3488646 A GB3488646 A GB 3488646A GB 3488646 A GB3488646 A GB 3488646A GB 633486 A GB633486 A GB 633486A
Authority
GB
United Kingdom
Prior art keywords
dimethylformamide
dianthraquinonylamide
reacted
chlorsulphonate
dibenzoylamino
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
GB3488646A
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.)
DAVID ALEXANDER WHYTE FAIRWEAT
Imperial Chemical Industries Ltd
Original Assignee
DAVID ALEXANDER WHYTE FAIRWEAT
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 DAVID ALEXANDER WHYTE FAIRWEAT, Imperial Chemical Industries Ltd filed Critical DAVID ALEXANDER WHYTE FAIRWEAT
Priority to GB3488646A priority Critical patent/GB633486A/en
Publication of GB633486A publication Critical patent/GB633486A/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
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/36—Dyes with acylated amino groups
    • C09B1/363—Dyes with acylated amino groups the acyl groups being residues of a dicarboxylic compound forming a bridge between two anthraquinones
    • 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
    • C09B9/00—Esters or ester-salts of leuco compounds of vat dyestuffs
    • C09B9/02—Esters or ester-salts of leuco compounds of vat dyestuffs of anthracene dyes

Abstract

Leuco-sulphuric esters of 1 : 11-di-anthraquinonylamides of dicarboxylic acids are made by treating the vat dye in presence of a metal, or treating a metal salt of a leuco-derivative of a vat dye, with a sulphating agent such as sulphur trioxide in presence of an amide derived from a secondary amine. Amides specified are dimethylformamide, diethylformamide, dimethylacetamide, tetramethylurea, N : N - diethyl - p - toluenesulphonamide. Acetone and acetonitrile are specified diluents. In examples: (1) terephthal-4 : 41-dibenzoylamino - 1 : 11 - dianthraquinonylamide is reacted with zinc dust and sodium-b -naphthalene sulphonate in dimethylformamide, and then with the addition product of dimethylformamide and methyl chlorsulphonate or sulphur trioxide; (2) terephthal-5 : 51-dibenzoylamino - 1 : 11 - dianthraquinonylamide is reacted with zinc dust, tetraethylammonium iodide and dimethylformamide, and then with dimethylformamide and methyl chlorsulphonate; (3) terephthal-1 : 11-dianthraquinonylamide is reacted with N-formomorpholide, acetone, zinc, and methyltriethylammonium chloride and then with methyl chlorsulphonate and more N-formomorpholide; (4) oxal-5 : 51-dibenzoylamino - 1 : 11 - dianthraquinonylamide is reacted with zinc, sodium b -naphthalene sulphonate, methyltriethylammonium chloride, and dimethylformamide, and then with dimethylformamide and sulphur trioxide. Specifications 274,156, [Class 2 (iii)], 476,255, 610,117, 633,481 and 633,513.
GB3488646A 1946-11-25 1946-11-25 Manufacture of new dyestuffs of the anthraquinone series Expired GB633486A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3488646A GB633486A (en) 1946-11-25 1946-11-25 Manufacture of new dyestuffs of the anthraquinone series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3488646A GB633486A (en) 1946-11-25 1946-11-25 Manufacture of new dyestuffs of the anthraquinone series

Publications (1)

Publication Number Publication Date
GB633486A true GB633486A (en) 1949-12-19

Family

ID=10371128

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3488646A Expired GB633486A (en) 1946-11-25 1946-11-25 Manufacture of new dyestuffs of the anthraquinone series

Country Status (1)

Country Link
GB (1) GB633486A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2727044A (en) * 1953-12-23 1955-12-13 Interchem Corp Yellow pigment

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2727044A (en) * 1953-12-23 1955-12-13 Interchem Corp Yellow pigment

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