GB1377697A - Disazo dyestuffs their preparation and use in photographic materials - Google Patents

Disazo dyestuffs their preparation and use in photographic materials

Info

Publication number
GB1377697A
GB1377697A GB1474172A GB1474172A GB1377697A GB 1377697 A GB1377697 A GB 1377697A GB 1474172 A GB1474172 A GB 1474172A GB 1474172 A GB1474172 A GB 1474172A GB 1377697 A GB1377697 A GB 1377697A
Authority
GB
United Kingdom
Prior art keywords
bis
give
chloroformyl
ethane
carboxy
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
GB1474172A
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of GB1377697A publication Critical patent/GB1377697A/en
Expired legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
    • G03G17/02—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process with electrolytic development
    • 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
    • C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/08—Preparation of azo dyes from other azo compounds by reduction
    • C09B43/085—Preparation of azo dyes from other azo compounds by reduction by reacting nitro azo dyes with amine or amino azo dye with nitro compounds
    • 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/145—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents with polycarboxylic acids
    • 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
    • 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
    • C09B45/00—Complex metal compounds of azo dyes
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/28—Silver dye bleach processes; Materials therefor; Preparing or processing such materials
    • G03C7/29—Azo dyes therefor

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Abstract

1377697 Carboxylic halides and intermediates therefor CIBA-GEIGY AG 29 March 1972 [14 May 1971] 14741/72 Heading C2C [Also in Divisions C4 and G2] 1 - (4<SP>1</SP> - Chloroformyl - benzamido) - 2 - chloro- 5-chloroformyl-benzene is prepared by condensing 3-amino-4-chlorobenzoic acid methyl ester with p-toluoylchloride to give 1-(4<SP>1</SP>-methylbenzamido) - 2 - chloro - 5 - methoxy carbonylbenzene which is hydrolysed with aq. NaOH to give 1 - (4<SP>1</SP> - methyl - benzamido) - 2 - chloro - 5- carboxy-benzene which is oxidized with KMnO 4 to give 1 - (4<SP>1</SP> - carboxy - benzamido) - 2 - chloro- 5 - carboxy - benzene which is finally treated with thionyl chloride. N - (3<SP>1</SP> - chloroformyl - phenyl) - 4 - chloroformylphthalimide is prepared by condensing trimellitic anhydride with 3-amino-benzoic acid to give N - (3<SP>1</SP> - carboxy - phenyl) - 4 - carboxyphthalimide and treating this with PCl 5 . 1,2 - Bis - (4 - chloroformyl - phenoxy)- ethane is prepared by condensing 4-hydroxybenzoic acid methyl ester with ethylene bromide to give 1,2 - bis - (4 - methoxycarbonyl - phenoxy)-ethane which is hydrolysed with aq. KOH to give 1,2 - bis - (4 - carboxy - phenoxy)- ethane which is treated with thionyl chloride. 1,3 - Bis - (4 - chloroformyl - phenylcarbonyl)- benzene is prepared by oxidizing 1,3-bis-(4- methyl-phenylcarbonyl)-benzene with KMnO 4 to give 1,3 - bis - (4 - carboxyphenyl - carbonyl)- benzene and treating this with PCl 5 . 1,2 - Bis - (4 - chloroformyl - benzamido)- ethane is prepared by condensing terephthalic acid monomethyl ester-monochloride with ethylene diamine to give 1,2-bis-(4-methoxycarbonylbenzamido)-ethane which is hydrolysed with aq. NaOH to give 1,2-bis-(4-carboxy-benzamido)- ethane and treating this with thionyl chloride. Further dichloroformyl compounds are listed in Table 1.
GB1474172A 1971-05-14 1972-03-29 Disazo dyestuffs their preparation and use in photographic materials Expired GB1377697A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH720871A CH566029A5 (en) 1971-05-14 1971-05-14

Publications (1)

Publication Number Publication Date
GB1377697A true GB1377697A (en) 1974-12-18

Family

ID=4321562

Family Applications (2)

Application Number Title Priority Date Filing Date
GB1474172A Expired GB1377697A (en) 1971-05-14 1972-03-29 Disazo dyestuffs their preparation and use in photographic materials
GB2054472A Expired GB1384162A (en) 1971-05-14 1972-05-03 Disazo dyestuffs their manufacture and use in photographic materials

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB2054472A Expired GB1384162A (en) 1971-05-14 1972-05-03 Disazo dyestuffs their manufacture and use in photographic materials

Country Status (9)

Country Link
JP (1) JPS5529419B1 (en)
AT (1) AT321718B (en)
BE (1) BE783388A (en)
CA (1) CA987309A (en)
CH (1) CH566029A5 (en)
DE (1) DE2223311A1 (en)
FR (1) FR2137637B1 (en)
GB (2) GB1377697A (en)
IT (1) IT957826B (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE624356A (en) * 1961-11-02 1963-04-30

Also Published As

Publication number Publication date
BE783388A (en) 1972-11-13
AT321718B (en) 1975-04-10
JPS5529419B1 (en) 1980-08-04
DE2223311A1 (en) 1972-11-30
CA987309A (en) 1976-04-13
FR2137637B1 (en) 1978-02-03
FR2137637A1 (en) 1972-12-29
CH566029A5 (en) 1975-08-29
IT957826B (en) 1973-10-20
GB1384162A (en) 1975-02-19

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee