GB784843A - New basic phthalocyanine dyestuffs and a process for their production - Google Patents
New basic phthalocyanine dyestuffs and a process for their productionInfo
- 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
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
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/12—Obtaining 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.
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)
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 |
-
1954
- 1954-12-21 GB GB36945/54A patent/GB784843A/en not_active Expired
Cited By (11)
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 |
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