GB517630A - Manufacture of new coloured organic compounds - Google Patents

Manufacture of new coloured organic compounds

Info

Publication number
GB517630A
GB517630A GB2284938A GB2284938A GB517630A GB 517630 A GB517630 A GB 517630A GB 2284938 A GB2284938 A GB 2284938A GB 2284938 A GB2284938 A GB 2284938A GB 517630 A GB517630 A GB 517630A
Authority
GB
United Kingdom
Prior art keywords
product
isoindolenylidene
bis
methylmercapto
give
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
GB2284938A
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.)
Imperial Chemical Industries Ltd
Original Assignee
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2284938A priority Critical patent/GB517630A/en
Publication of GB517630A publication Critical patent/GB517630A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Indole Compounds (AREA)

Abstract

517,630. Dyes.. DAVIES, J. S. H., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. Aug. 2, 1938, No. 22849. [Class 2 (iii)] New coloured compounds are obtained by treating the products of Specification 516,342, or their mono or dialkyl thio ethers with organic compounds which are wholly or partly cyclic and which include the atomic grouping -CN2.CO-. Pyrazolones, thioindoxyls and those naphthols and phenols which are capable of reacting as ketones are preferred compounds having the atomic grouping -CH2.CO-. Either one or both mercapto or alkylmercapto substituents are replaced by radicals of the compounds containing this grouping. The condensation is conveniently effected by heating the reactants together, preferably in a liquid such as dimethylaniline or monochloronaphthalene. Those products which are obtained from starting materials containing the -CN2.CO- grouping and also containing aryl radicals or other nuclei, which can be sulphonated, can be converted to water-soluble derivatives by sulphonation with concentrated sulphuric acid or oleum, if necessary at a raised temperature. The insoluble products can be used as pigment dyes and usually also as vat dyes. The soluble products can be used as bases for lakes and as dyestuffs for wool and cotton. In the examples, (1) alpha - naphthol, 1:1<1> - di(methylmercapto) - 3:3<1> - bis - isoindolenylidene (made by treating the product of example (1) of Specification 516,342, with dimethylsulphate and alkali) and dimethylaniline are heated together to give a product which when dissolved in aqueous alkaline hydrosulphite solution dyes cotton a greenish-blue shade. The same product is obtained from 1:1<1> - di-(ethylmercapto)-bis-isoindolenylidene; (2) a-naphthol is heated with the product of example (1) of Specification 516,342, to give the same product as in example (1); (3) the product of example (1) is sulphonated to give a product which dyes wool greenishblue shades ; (4) tetrachloro- or diamino-1:1<1>- dimercapto - 3:3<1> - bis - isoindolenylidene, Specification 516,342, alpha-naphthol and monochloronaphthalene are heated together to give products similar to that of example (2); (5) 1:1<1> - di - (methylmercapto) - 3:3<1> - bis - isoindolenylidene is condensed with the following compounds, the products being subsequently sulphonated : the colours which these sulphonated products give on wool are indicated in brackets: (a) 4 chloro-1-naphthol (bluishgreen), (b) 5 - methoxy - 1 - naphthol (green), (c) 5 - methylamino - 1 - naphthol, (d) 5 - # - hydroxy - ethylamino - 1 - naphthol (grey), (e) 1:5 - dihydroxynaphthalene (bluish - green), (f) 1:8 - dihydroxynaphthalene (green), (g) resorcinol (bluish-grey), (h) hydroxynaphthocarbazole (reddish-grey), (j) 2:4-diketo-1:2:3:4- tetrahydroquinoline; (k) 1:3-diketo-1:2:3:4:- tetrahydro-isoquinoline and (1) 1:4-diketo- 1:2:3:4:-tetrahydro - isoquinoline ; the unsulphonated products dye cotton shades from bluish-grey to reddish-grey from alkaline hydrosulphite vats ; (6) 2-hydroxy-3-naphthoic anilide, 1:1<1>-di-(methylmercapto)-3:3<1>-bis-isoindolenylidene and monochlornaphthalene are heated together, the product dyes cotton green shades from an alkaline hydrosulphite vat; (7) 6 - ethoxythioindoxyl, 1:1<1> - di - (methylmercapto) - 3:3<1> - bis - isoindolenylidene and dimethylaniline are heated together ; (8) the product of example (7) is sulphonated ; (9) the product of example (7) is also made by heating the product of example (1) of Specification 516,342, 6-ethoxythioindoxyl and monochloronaphthalene together; (10) 2:1-naphthathioindoxyl, 1:1<1> - di - (methylmercapto) - 3:3<1> - bis - isoindolenylidene and dimethylaniline are heated together to give a product which dyes cotton in green shades from an alkaline hydrosulpnite vat; (11) the product of example (10) is sulphonated to give a compound which dyes wool green shades ; (12) 1:11 - di- (methylmer - capto) - 3:3<1> - bis - isoindolenylidene is heated with the following thioindoxyls (the colours which the sulphonated products give on wool are indicated in brackets): (a) thioindoxyl (bluish-green), (b) 5 - chloro - 7 - methylthioindoxyl (yellowish - green), (c) 6 - chloro - 4 - methylthioindoxyl (greenish-blue), 1:2 - naphthathioindoxyl (greenish - blue) and 2:3 - naphthathioindoxyl (yellowish - green); (13) 1:1<1> - di - (methylmercapto) - 3:3<1> - bis - isoindolenylidene and dimethylaniline are heated together ; (14) 1-phenyl-3-methyl-5-pyrazolone, 1:11 - di - (methylmercapto) - 3:3<1> - bi's - iso - indolenylidene and dimethylaniline are heated together to give a product which dyes cotton violet shades from an alkaline hydrosulphite vat, (15) the product of example (14) is sulphonated; (16) 1 - (4' - nitro) - phenyl - 3 - methyl - 5 - pyrazolone, 1:1<1> - di - (methylmercapto) - 3:31 - bis - isoindolenylidene and dimethylaniline are heated together; (17) rhodanine, 1:1<1> - di - (methylmercapto) - 3:3<1> - bis - isoindolenylidene and dimethylaniline are heated together.
GB2284938A 1938-08-02 1938-08-02 Manufacture of new coloured organic compounds Expired GB517630A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2284938A GB517630A (en) 1938-08-02 1938-08-02 Manufacture of new coloured organic compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2284938A GB517630A (en) 1938-08-02 1938-08-02 Manufacture of new coloured organic compounds

Publications (1)

Publication Number Publication Date
GB517630A true GB517630A (en) 1940-02-05

Family

ID=10186028

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2284938A Expired GB517630A (en) 1938-08-02 1938-08-02 Manufacture of new coloured organic compounds

Country Status (1)

Country Link
GB (1) GB517630A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3330834A (en) * 1967-07-11 Naphthalimide whitening agents anb method of making same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3330834A (en) * 1967-07-11 Naphthalimide whitening agents anb method of making same

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