GB784843A - New basic phthalocyanine dyestuffs and a process for their production - Google Patents

New basic phthalocyanine dyestuffs and a process for their production

Info

Publication number
GB784843A
GB784843A GB36945/54A GB3694554A GB784843A GB 784843 A GB784843 A GB 784843A GB 36945/54 A GB36945/54 A GB 36945/54A GB 3694554 A GB3694554 A GB 3694554A GB 784843 A GB784843 A GB 784843A
Authority
GB
United Kingdom
Prior art keywords
amino
phthalocyanine
acid
diethylamino
pentane
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
GB36945/54A
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB784843A publication Critical patent/GB784843A/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
    • C09B47/00Porphines; Azaporphines
    • C09B47/04Phthalocyanines abbreviation: Pc
    • C09B47/08Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
    • C09B47/12Obtaining compounds having alkyl radicals, or alkyl radicals substituted by hetero atoms, bound to the phthalocyanine skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

The invention comprises basic phthalocyanine dyestuffs having one to four radicals of formula: <FORM:0784843/IV (b)/1> attached to a phthalocyanine radical, wherein R1 is an hydrogen atom or an alkyl radical, R2 is an acyclic bivalent radical which may contain a further <FORM:0784843/IV (b)/2> group and R3 and R4 are aliphatic radicals or together with the adjacent nitrogen atom form a heterocyclic ring. The dyestuffs may be prepared by reacting a phthalocyanine dyestuff which contains one to four replaceable halogen atoms (a) with a tertiary amine of formula: <FORM:0784843/IV (b)/3> wherein R1 to R4 have the aforementioned meanings, or (b) with an aliphatic primary or secondary amine containing at least one halogen atom and reacting the halogen compound thus prepared with a secondary amine. Method (b) may give dyestuffs wherein R1 is an <FORM:0784843/IV (b)/4> group. Dyestuffs containing carboxylic acid halide, sulphonic acid halide or halogenoalkyl groups may be used as starting materials. Specified tertiary amines for use in method (a) are 1-amino-2-dimethylamino-ethane, 1-amino-3 - dimethylaminopropane, 1 - diethylamino-3-amino-n-pentane and the amide of methyl-aminoacetic acid and 1-diethylamino-4-amino-n-pentane. Specified halogen-containing amines for use in method (b) are b -chloro-ethylamine, b : g - dibromopropylamine, 1 - amino - 4 - chlorobutane and b : b 1 - dichlorodiethylamine. Specified secondary amines for use in method (b) are dimethyl-, diethyl- and diethanolamines, piperidine, pyrrolidine and pyrroline. Instead of using phthalocyanine dyestuffs, intermediates containing a replaceable halogen atom, which upon completion of the above reactions are converted into phthalocyanine dyestuffs, may be used. The reaction medium may be an excess of the base employed in the reaction, an inert organic solvent such as benzene or acetone, or water. Acid-binding agents such as an excess of the base, an alkali metal carbonate, sodium hydroxide or sodium bicarbonate may be present. Reaction temperatures between 0-100 DEG C. are specified. The dyestuffs may be used to dye plastics, varnishes, cotton, cellulose materials, wool, polyamides or polyacrylonitrile. In examples: (1) copper or nickel phthalocyanine is treated with a mixture of chlorosulphonic acid and thionyl chloride to give the corresponding -(3)-di- or tri-sulphochloride which is reacted with 1 - amino - 2 - dimethylamino - ethane, or 1-amino - 3 - dimethylamino - propane, or 1-diethylamino - 4 - amino - n - pentane or the amide of methylaminoacetic acid and 1-diethyl-amino - 4 - amino - n - pentane; (2) copper phthalocyanine-4 : 41-disulphonic acid is treated with a mixture of chlorosulphonic acid and thionyl chloride and the resultant sulphochloride reacted with 1-amino-3-dimethylaminopropane or 1-amino-2-dimethylamino-ethane; (3) as in (2) using 3 : 31-diaza - copper phthalocyanine-4 : 41-disulphonic acid and 1-diethylamino-4-amino-n-pentane; (4) as in (2) using 4 : 41 - diphenyl - copper phthalocyanine-411 : 4111-disulphonic acid and 1-amino-3-dimethylamino-propane; (5) as in (2) using 4 : 41 : 411 : 4111 - tetraphenyl - copper phthalocyanine and 1 - diethylamino - 4 - amino - n-pentane; (6) as in (2) using cobalt phthalocyanine - 4 : 41 : 411 : 4111 - tetrasulphonic acid and 1-amino-3-dimethylamino-propane or 1-diethylamino-4-amino-n-pentane; (7) a copper phthalocyanine containing three or four chloromethyl groups is reacted with 1-diethylamino-4-amino-n-pentane; (8) as in (2) using a copper phthalocyanine obtained from diphenylsuphone-3 : 4-dicarboxylic acid-31-sulphonic acid and 1-amino-2-dimethylamino-ethane; (9) as in (2) using 4 : 41 : 411 : 4111 : 5 : 51 511 : 5111-octaphenyl copper phthalocyanine and 1-amino-2-diethylamino-ethane; (10) copper phthalocyanine - (3) - di - and - tri - sulphochloride is reacted with b -chloroethylamine and the resultant sulphonamide reacted further with dimethylamine or diethylamine or diethanolamine or 1-amino-3-dimethylaminopropane; (11) as in (10) but using 2 : 3-dibromopropylamine and dimethylamine; (12) as in (10) using 4 : 41 : 411 : 4111-copper phthalocyanine - tetra - (p - phenyl - sulphochloride) or -sulphochloride, b -chloroethylamine and dimethylamine.
GB36945/54A 1953-12-21 1954-12-21 New basic phthalocyanine dyestuffs and a process for their production Expired GB784843A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE784843X 1953-12-21

Publications (1)

Publication Number Publication Date
GB784843A true GB784843A (en) 1957-10-16

Family

ID=6698620

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36945/54A Expired GB784843A (en) 1953-12-21 1954-12-21 New basic phthalocyanine dyestuffs and a process for their production

Country Status (1)

Country Link
GB (1) GB784843A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102980A (en) * 1990-11-13 1992-04-07 Eastman Kodak Company Colored polyester compositions
EP0699720A1 (en) 1994-08-24 1996-03-06 Bayer Corporation Process for preparing alpha-phase metal phtalocyanine pigments
GB2371300A (en) * 2000-11-17 2002-07-24 Council Scient Ind Res Metal Phthalocyanine Sulfonamides and their use as sweeteners for LPG and light petroleum distillates
US7182806B2 (en) 2003-07-18 2007-02-27 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
US7189283B2 (en) 2003-07-18 2007-03-13 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
US7326287B2 (en) 2003-07-18 2008-02-05 Fujifilm Imaging Colorants Limited Cyan inks and their use in ink-jet printers
US7678899B2 (en) 2003-07-18 2010-03-16 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
CN106083864A (en) * 2016-06-14 2016-11-09 浙江永太新材料有限公司 A kind of preparation method of CuPc blue color basic inductor compound

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102980A (en) * 1990-11-13 1992-04-07 Eastman Kodak Company Colored polyester compositions
EP0699720A1 (en) 1994-08-24 1996-03-06 Bayer Corporation Process for preparing alpha-phase metal phtalocyanine pigments
US5534055A (en) * 1994-08-24 1996-07-09 Bayer Corporation Process for alpha-phase metal phthalocyanine pigments
GB2371300A (en) * 2000-11-17 2002-07-24 Council Scient Ind Res Metal Phthalocyanine Sulfonamides and their use as sweeteners for LPG and light petroleum distillates
GB2371300B (en) * 2000-11-17 2004-08-04 Council Scient Ind Res Process for the preparation of metal phthalocyanine tetrasulphonamide sweeting catalysts
US7182806B2 (en) 2003-07-18 2007-02-27 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
US7189283B2 (en) 2003-07-18 2007-03-13 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
US7326287B2 (en) 2003-07-18 2008-02-05 Fujifilm Imaging Colorants Limited Cyan inks and their use in ink-jet printers
US7678899B2 (en) 2003-07-18 2010-03-16 Fujifilm Imaging Colorants Limited Phthalocyanines and their use in ink-jet printers
CN106083864A (en) * 2016-06-14 2016-11-09 浙江永太新材料有限公司 A kind of preparation method of CuPc blue color basic inductor compound
CN106083864B (en) * 2016-06-14 2018-06-08 浙江永太新材料有限公司 A kind of preparation method of CuPc blue color basic inductor compound

Similar Documents

Publication Publication Date Title
GB784843A (en) New basic phthalocyanine dyestuffs and a process for their production
US2334186A (en) Organic sulphonamides and their preparation
GB1114427A (en) Azophthalocyanine dyestuffs and processes for their manufacture
US3892807A (en) Aromatic azomethines
US2086822A (en) Process for producing aromatic asymmetrical thiourea derivatives
ES466195A1 (en) Concentrated, aqueous solutions of salts of acetoacetylamino-arylsulphonic acids and method of forming concentrated solutions of azo dyestuffs therefrom
US2581443A (en) Preparation of n-substituted nitrogen heterocyclic bases
ES436558A1 (en) Process for the synthesis of substituted indolenines
US3972894A (en) Synthesis of oxindoles from anilines and β-thio carboxylic esters or amides
GB872561A (en) Process for the manufacture of dyestuffs of the triphenylamino triphenylmethane series
US2779766A (en) Pyrroles having amino, cyano, and mercapto or substituted mercapto groups and their preparation
DE2234207A1 (en) N-SUBSTITUTED IMINOCUMARIN COLORS
US2524084A (en) Peroxidic sulfonic acids and salts
US3775442A (en) Process for the manufacture of a triarylmethane compound
GB978550A (en) Acylacetylaminobenzene compounds containing sulphonic acid groups and process for their manufacture
US2063191A (en) Hydroxy phenyl morpholines
US2553475A (en) Manufacture of dyestuffs
US2426882A (en) Sulfonyl dicyandiamides and methods for their preparation
GB950698A (en) New dyes containing dihalopyridazone groups
US2902487A (en) Process of preparing 8-amino-1-napththo-sulfonamides
GB1215396A (en) Production of monothio-oxamic acid compounds
CH637912A5 (en) METHOD FOR PRODUCING AMINES.
GB1123762A (en) Improved process for the production of 5-cyano-uracil compounds and new intermediate products that can be formed thereby
GB786567A (en) Metallisable heterocyclic azo dyestuffs
US2041716A (en) Amino-ortho-nitro-aryl-thiocarboxylic acids, and process of preparing same