Production of a monochloro copper phthalocyanine pigment

    公开(公告)号:GB1073348A

    公开(公告)日:1967-06-21

    申请号:GB4169464

    申请日:1964-10-13

    Applicant: BASF AG

    Abstract: Monochloro copper phthalocyanine is produced by heating phthalodinitrile and copper (II) chloride in nitrobenzene in the presence of 0.05-0.5 mole of a tertiary aromatic base to each mole of CuCl2 at 195-211 DEG C. The ratio of phthalodinitrile to CuCl2 is preferably 4:1 to 3.5:1 and the specified bases are pyridine, piccolines, isoquinoline and, especially, quinoline. Examples are given.

    New phthalocyanine dyes
    7.
    发明专利

    公开(公告)号:GB919179A

    公开(公告)日:1963-02-20

    申请号:GB3522660

    申请日:1960-10-14

    Applicant: BASF AG

    Abstract: 1-Amino-4-chloro- or -bromo-butine-(2), 1-amino - 4 - chlorobutene - (2), 1-amino-3 : 4-dichlorobutene-(2) and 1-amino-2 : 3-dimethyl-4-bromobutene-(2) hydrochlorides are made by treating methanolic hydrogen chloride the reaction product of the appropriate dihalobutene or butine with hexamethylene tetramine. The hydrochlorides of 1-(4-aminophenoxy)-3 : 4-dichlorobutene-(2), 1-(4-aminophenoxy)-4-chlorobutine - (2), 1-aminobenzene-3-sulphonic acid-(3 : 4-dichlorobuten-(2)-ylamide) and of 1-aminobenzene-4-sulphonamide substituted in the amide group by 3 : 4-dichlorobuten-(2)-yl, 4-chlorobuten-(2)-yl and 4-chlorobutin-(2)-yl radicals are made by hydrolysis of the corresponding acetylamino compounds. 2-(4-chlorobutin - (2) - ylamino - (1))-4 : 6-dichloro-1 : 3 : 5-triazine is made by reacting cyanuric chloride with 1-amino-4-chlorobutine. Benzene-1-sulphonic acid-(4-chlorobutin-(2)-ylamide)-3- and -4-carboxylic acid chlorides are made from the corresponding carboxylic acids prepared by reacting the corresponding benzoic acid sulphochloride with 1-amino-4- chlorobutine-(2). Specification 827,569 is referred to.ALSO:The invention comprises dyes of the formula:-(HO3S)n-(-Pc-)-(A-E-F)m where Pc is the radical of a metal-free or metalliferous phthalocyanine, or of a chlorphthalocyanine, phenylphahalocyanine, phenylmercaptophthalocyanine or phenylsulphonylphthalocyanine containing 1 to 4 chloro, phenyl, phenylmercapto or phenylsulphonyl radicals in the molecule and wherein the metal of the metalliferous derivatives is not lost by treatment with concentrated sulphuric acid at room temperature, A is one of the radicals -SO2-NH- E is -CH2C=C-CH2 or CH2-C=C-CH2-, R1 and R2 are each hydrogen, chlorine, bromine or methyl, X is hydrogen or sulphonic acid, F is chlorine or bromine or one of the radicals -O-SO3H, Q is a chlorine or bromine ion, n is 0-4 and m is 1-4. The dyes are made by reacting a phthalocyanine amine of the formula:-(HO3S)n-(Pc)-(D)m with m mols of a compound Y-E-Z where Pc, E, n and m are as above, Z is chlorine, bromine or -OSO3H, D is -NH2, -CH2NH2, or and Y is chlorine or bromine or when D is Y may also be or or by reacting a phthalocyanine sulphonchloride of the formula (Pc)-(SO2T)m + n with m mols of H2N-G-E-Z and hydrolysing the remaining sulphonchloride groups, where Pc, E, Z, m and n are as above, T is chlorine or bromine and G is a covalent linkage or or or by reacting a derivative of the formula (HO3S)n-(Pc)-(L-T)m with m mols of H2N-E-Z where Pc, T, E, Z, m and n are as above and L is or When Z in the above products is chlorine or bromine they may optionally be reacted with pyridine or tetramethylthiourea. Examples are given. The dyes dye and print textile materials of wool, silk, synthetic linear polyamides and leather, and dye and print natural or regenerated cellulose textile materials in conjunction with an alkali and heat treatment. Specification 827,569 is referred to.

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