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GB465200A - Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur - Google Patents

Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur

Info

Publication number
GB465200A
GB465200A GB2382435A GB2382435A GB465200A GB 465200 A GB465200 A GB 465200A GB 2382435 A GB2382435 A GB 2382435A GB 2382435 A GB2382435 A GB 2382435A GB 465200 A GB465200 A GB 465200A
Authority
GB
United Kingdom
Prior art keywords
compounds
quaternary ammonium
treated
products
dimethylsulphate
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
GB2382435A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB2382435A priority Critical patent/GB465200A/en
Publication of GB465200A publication Critical patent/GB465200A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C381/00Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
    • C07C381/12Sulfonium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/54Quaternary phosphonium compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/607Nitrogen-containing polyethers or their quaternary derivatives
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/607Nitrogen-containing polyethers or their quaternary derivatives
    • D06P1/6076Nitrogen-containing polyethers or their quaternary derivatives addition products of amines and alkylene oxides or oxiranes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/613Polyethers without nitrogen
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/655Compounds containing ammonium groups
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/655Compounds containing ammonium groups
    • D06P1/66Compounds containing ammonium groups containing quaternary ammonium groups
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/13Fugitive dyeing or stripping dyes
    • D06P5/138Fugitive dyeing or stripping dyes fugitive dyeing

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paper (AREA)

Abstract

Products useful as assistants in the textile, paper, lacquer, tanning and rubber industries are obtained by introducing one or more ether or polyether radicles into quaternary ammonium or phosphonium compounds or ternary sulphonium compounds by condensing the latter with polyhydric alcohols or etherifying derivatives thereof having at most six carbon atoms or with polyether compounds containing atoms or groups such as halogen which react with the said quaternary ammonium or phosphonium or ternary sulphonium compounds. Specified components are: ethylene and propylene oxides, glycide, epichlorhydrin, dichlorhydrin, dichlordiethylether, glycol, glycerol, polyglycerol, glycolchlorhydrin, polyglycerolchloride and a -chlor tetraethylene glycol. The quaternary phosphonium and ammonium compounds and the ternary sulphonium compounds may contain hydroxyl, carboxylic, amino or mercapto groups which react with the second components. The same products may also be produced from any compound containing nitrogen, phosphorus or sulphur by first introducing the ether group or groups and then converting the resulting ethers into quaternary ammonium or ternary sulphonium compounds. Thus, diethylbutanolamine, asymdimethylethylenediamine or sarcosine may be treated with ethyleneoxide and quaternary ammonium compounds produced by a final treatment with dimethylsulphate, ethylbromide or benzylchloride. The following starting materials which contain radicles of high molecular weight are advantageously employed: dodecyldimethyl hydroxyethylammoniumhydroxide, stearyltrihydroxyethyl ammoniumhydroxide, dimethyloxyethyldibutylammoniumhydroxide, the monooleicester of tetrahydroxyethylammoniumhydroxide, dodecyldimethylcarboxymethylammoniumchloride (from dodecyldimethylamine and chloracetic acid), the reaction product of ethylenediamine with octodecyldimethylchlorethylammoniumchloride (from octodecyldimethylamine and ethylenechloride), the reaction product of dimethyl sulphate with stearyldiethylenetriamine, the quaternary ammonium compounds of oleylpiperazine (from piperazine and oleylsulphuric ester), quaternary ammonium compounds obtained by adding on dodecyl bromide, dodecahydroxymethylchloride or dodecathio methylchloride to tetramethyl-b -hydroxypropylenediamine, oleyldihydroxyethylamineoxide (from oleylamine, ethyleneoxide and hydrogen peroxide), stearylamine, oleylamine, dodecylmethylamine, didodecylamine, octodecylethylenediamine, dodecylpropylenediamine, and polyether derivatives of oleic acid amides of ethylenediamine, triethylenetetramine or ethylene diaminosorbitol (from glucose and ethylenediamine followed by reduction) and polyether derivatives of the reaction product of triethylenetetramine or aminosorbitol with trichlorinated paraffin wax or of oleylamide of piperazine. The high molecular radicle may however be introduced when the ethers are converted into quaternary ammonium or ternary sulphonium compounds. The products may be condensed with chlorethane sulphonic acid, chloracetic acid, fatty acid chlorides, chlorcarbonic esters, isocyanates or treated with phosphoric acid or sulphonating agents. The wetting, dispersing, levelling, washing and softening properties of the products make them useful in the following processes; bleaching, bucking, carbonizing, mercerizing, stripping, printing, mordanting, fulling, dressing, waterproofing, crease-proofing and combating pests. They may also be added to artificial silk spinning solutions, lubricants, textile oils, shoe polishes, pharmaceutical products, cosmetics and flotation agents. They may be used in dyeing with acetate artificial silk dyes, and with vat, acid, substantive and basic dyes. The products may be used in association with soaps, sulphuric esters and sulphonic acids, condensation products of fatty acid chlorides with albumen degradation products, aminocarboxylic acids, condensation products of alkyleneoxides with hydroxy, carboxy, amino or mercapto compounds, starch, dextrine, cellulose derivatives, sulphite cellulose, ortho-, pyro- or meta-phosphates, Glauber's salts, glue, mucilages, resins, waxes, oils, fats, solvents, cyclohexanol, hydrogen peroxide and other per compounds and reducing agents such as sodium hydrosulphite. In examples: (1) stearylamine is treated with ethylene oxide and a quaternary ammonium compound formed by means of dimethylsulphate; the product may be added to bottoming or developing baths in dyeing with azo dyestuffs: (2) ethylenediamine or b : b -dibutyl ethylenediamine is treated with ethyleneoxide and a quaternary ammonium compound formed with octodecylbromide: (3) dodecyldimethylhydroxyethylammoniumhydroxide or stearyl trihydroxyethylammonium hydroxide is treated with ethylene oxide; a soap of stearylamine and stearic acid is treated with ethyleneoxide or a salt with stearic acid is formed from the quaternary ammonium base obtained from stearyltrihydroxyethylammonium hydroxide and ethylene oxide: (4) propylene oxide is reacted with tetrahydroxyethylammonium hydroxide: (5) methyldodecylamine is treated first with ethylene oxide and then with dimethylsulphate; the product may be used in dyeing with Naphthol AS. and as an assistant in association with oleylsarcosine in bleaching with sodium hydrosulphite: (6) quaternary ammonium compounds are obtained by treating with dimethylsulphate the products obtained from oleylamine and ethyleneoxide: (7) dimethylsulphate is added to the condensation product of oleylamine and ethylene oxide and the resulting quaternary salt sulphonated; the product may be used for dyeing mercerized calico with Hydronblau R: (8) stearylamine is treated first with ethyleneoxide and then with ethylene chlorhydrin; the product which may be used with enzyme preparations may be used for washing wool or cotton: (9) an amide obtained from ethylenediamine or phenylenediamine and oleic acid or dodecylpropylenediamine or paraaminophenol is treated with ethyleneoxide and a quaternary ammonium salt formed with dimethylsulphate. Specification 420,066 is referred to. Samples have been furnished under Sect. 2 (5) of products prepared as follows: (1) triphenylphosphine is heated with ethylenechlorhydrin in the presence of potassium iodide and a quaternary phosphonium base formed by treating with ethyleneoxide: (2) ethylenediamine is treated with ethylene oxide and high molecular residues of palm kernel oil introduced into the resulting quaternary base, which is finally sulphonated: (3) ethylenediamine is condensed with chloracetic acid, and the reaction product treated first with ethylene oxide and then with dimethylsulphate: (4) dodecylmercaptan is treated with ethyleneoxide and dimethylsulphate; a sulphonium base is obtained by boiling with caustic soda: (5) benzyl mercaptan is treated with ethyleneoxide and dimethylsulphate; a sulphonium base results on adding caustic soda. Dodecylhydroxy- and dodecylthio-methylchloride are obtained by reacting dodecylalcohol or dodecylmercaptan with formaldehyde in the presence of hydrogen chloride. Reference has been directed by the Comptroller to Specification 441,473.ALSO:Products stated to have dispersing properties are obtained by introducing one or more ether or poly ether radicles into quaternary ammonium or phosphonium compounds or ternary sulphonium compounds by condensing the latter with polyhydric alcohols or etherifying derivatives thereof having at most six carbon atoms or with polyether compounds containing atoms or groups such as halogen, which react with the said quarternary ammonium or phosphonium or ternary sulphonium compounds. Specified components are: ethylene and propylene oxides, glycide, epichlorhydrin, dichlorhydrin, dichlordiethylether, glycol, glycerol, polyglycerol, glycolchlorhydrin and polyglycerolchloride. The quaternary phosphonium and ammonium compounds and the ternary sulphonium compounds may contain hydroxyl, carboxylic, amino or mercapto groups which react with the second components. The same products may also be produced from any compound containing nitrogen, phosphorus or sulphur by first introducing the ether group or groups and then converting the resulting ethers into quaternary ammonium or ternary sulphonium compounds. Thus, diethylbutanolamine, asym-dimethylethylenediamine or sarcosine may be treated with ethyleneoxide and quaternary ammonium compounds produced by a final treatment with dimethylsulphate, ethylbromide or benzylchloride. The following starting materials which contain radicles of high molecular weight are advantageously employed: dodecyldimethylhydroxyethylammoniumhydroxide, stearyltrihydroxyethylammonium hydroxide, dimethyloxyethyldibutyl ammoniumhydroxide, the monooleic ester of tetrahydroxyethylammoniumhydroxide, dodecyldimethylcarboxymethylammoniumchloride, the reaction product of ethylenediamine with octodecyldimethylchloroethylammoniumchloride, the reaction product of dimethylsulphate with stearyldiethylenetriamine, the quaternary ammonium compounds of oleylpiperazine, quaternary ammonium compounds obtained by adding on dodecyl bromide, dodecahydroxymethylchloride or dodecathiomethylchloride to tetramethyl-b -hydroxypropylenediamine, oleyldi--hydroxyethylamineoxide, stearylamine, oleylamine, dodecylmethylamine, didodecylamine, octodecylethylenediamine, dodecylpropylene - diamine, and polyether derivatives of oleic acid amides of ethylenediamine, triethylenetetramine or ethylene diaminosorbitol and poly ether derivatives of the reaction product of triethylenetetramine or aminosorbitol with trichlorinated paraffin wax or of the oleylamide of piperazine. The high molecular radicle may however be introduced when the ethers are converted into quaternary ammonium or ternary sulphonium compounds. The products may be condensed with chlorethanesulphonic acid, chloracetic acid, fatty acid chloride, chlorcarbonic esters, isocyanates or treated with phosphoric acid o
GB2382435A 1935-08-26 1935-08-26 Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur Expired GB465200A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2382435A GB465200A (en) 1935-08-26 1935-08-26 Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2382435A GB465200A (en) 1935-08-26 1935-08-26 Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur

Publications (1)

Publication Number Publication Date
GB465200A true GB465200A (en) 1937-04-26

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE879388C (en) * 1938-05-15 1953-06-11 Hoechst Ag Process for the preparation of quaternary ammonium salts
US3333005A (en) * 1963-06-04 1967-07-25 American Cyanamid Co Quaternary organophosphonium halides and preparation thereof
US3919283A (en) * 1965-03-18 1975-11-11 Ciba Geigy Ag Sulfate derivatives of polyglycol compounds
US3958931A (en) * 1965-03-18 1976-05-25 Ciba-Geigy Ag Wool dyeing with epihalohydrin or chloroacetamide quarternized polyglycolamine assisted dye solution
US4132657A (en) 1973-04-09 1979-01-02 Gaf Corporation Treatment of metal surfaces
US4138371A (en) 1976-04-07 1979-02-06 Gaf Corporation Washing method using amphoteric surface active agents
GB2133028A (en) * 1982-12-23 1984-07-18 Procter & Gamble Detergent compositions
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
US4551506A (en) 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
GB2168364A (en) * 1984-12-14 1986-06-18 Sandoz Ltd Sulphates of oxyalkylated amines and their use as dyeing assistants
US4597898A (en) * 1982-12-23 1986-07-01 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
GB2180249A (en) * 1982-12-23 1987-03-25 Procter & Gamble Ethoxylated polyamino compounds
US4659802A (en) 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
US4661288A (en) 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
EP0665325A2 (en) * 1994-01-26 1995-08-02 Hoechst Aktiengesellschaft Process for the manufacture of aminated cotton fibers

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE879388C (en) * 1938-05-15 1953-06-11 Hoechst Ag Process for the preparation of quaternary ammonium salts
US3333005A (en) * 1963-06-04 1967-07-25 American Cyanamid Co Quaternary organophosphonium halides and preparation thereof
US3919283A (en) * 1965-03-18 1975-11-11 Ciba Geigy Ag Sulfate derivatives of polyglycol compounds
US3958931A (en) * 1965-03-18 1976-05-25 Ciba-Geigy Ag Wool dyeing with epihalohydrin or chloroacetamide quarternized polyglycolamine assisted dye solution
US4132657A (en) 1973-04-09 1979-01-02 Gaf Corporation Treatment of metal surfaces
US4138371A (en) 1976-04-07 1979-02-06 Gaf Corporation Washing method using amphoteric surface active agents
US4551506A (en) 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
GB2133028A (en) * 1982-12-23 1984-07-18 Procter & Gamble Detergent compositions
GB2168708A (en) * 1982-12-23 1986-06-25 Procter & Gamble Quaternany ammonium compounds
US4597898A (en) * 1982-12-23 1986-07-01 The Proctor & Gamble Company Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties
GB2180249A (en) * 1982-12-23 1987-03-25 Procter & Gamble Ethoxylated polyamino compounds
US4659802A (en) 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
US4661288A (en) 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
GB2168364A (en) * 1984-12-14 1986-06-18 Sandoz Ltd Sulphates of oxyalkylated amines and their use as dyeing assistants
EP0665325A2 (en) * 1994-01-26 1995-08-02 Hoechst Aktiengesellschaft Process for the manufacture of aminated cotton fibers
EP0665325A3 (en) * 1994-01-26 1997-10-22 Hoechst Ag Process for the manufacture of aminated cotton fibers.

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