GB869423A - Manufacture of polyquaternary compounds - Google Patents

Manufacture of polyquaternary compounds

Info

Publication number
GB869423A
GB869423A GB27955/57A GB2795557A GB869423A GB 869423 A GB869423 A GB 869423A GB 27955/57 A GB27955/57 A GB 27955/57A GB 2795557 A GB2795557 A GB 2795557A GB 869423 A GB869423 A GB 869423A
Authority
GB
United Kingdom
Prior art keywords
denotes
radicals
piperidine
hydrocarbon radicals
products
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
GB27955/57A
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 GB869423A publication Critical patent/GB869423A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02Polyamines
    • C08G73/0206Polyalkylene(poly)amines
    • C08G73/0213Preparatory process
    • C08G73/0226Quaternisation of polyalkylene(poly)amines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Resinous polyquaternary compounds are produced by a process in which a monohalogenated tertiary amine of the general formula: <FORM:0869423/IV (a)/1> wherein R1 and R2 denote similar or different hydrocarbon radicals or R1 and R2 together with the nitrogen atom and possibly another hetero atom form a heterocyclic radical, R3 denotes a hydrocarbon radical which may contain one or more heteroatoms and X denotes a halogen atom is contacted with water, preferably with stirring and warming, in an amount insufficient to form a homogeneous system with the amine. The products are employed in aqueous solution as after-treatment agents for dyed materials (see Group IV(c)). The monovalent hydrocarbon radicals specified include alkyl, cycloalkyl, aryl and aralkyl radicals and heteocyclic radicals specified include pyrrolidone, piperidine and hexamethylene imine. Among specific products mentioned are those prepared from diethylchlorethylamine, N-chlorethyl hexamethylene imine, the chlorethyl derivatives of morpholine, piperidine, pyrrolidine and ethyl hexahydroaniline, di-isobutyl-chloroethylamine and b -chloro-b 1-diethylamino-diethyl ether.ALSO:A process for the production of polyquaternary compounds is characterised in that a monohalogenated tertiary amine of the general formula: <FORM:0869423/IV (b)/1> wherein R1 and R2 denote similar or different hydrocarbon radicals, or R1 and R2 together with the nitrogen atom and possibly another hetero atom form a heterocyclic radical, R3 denotes a hydrocarbon radical which may contain one or more heteroatoms and X denotes a halogen atom is contacted with water, preferably with stirring, and warming, in an amount insufficient to form a homogeneous system with the amine. The products are employed in aqueous solution as after-treatment agents for dyed materials (see Group IV(c)). The monovalent hydrocarbon radicals specified include alkyl, cycloalkyl, aryl and aralkyl radicals and heterocyclic radicals specified include pyrrolidine, piperidine and hexamethylene imine. Among the products specified are those prepared from diethylchloroethylamine, N-chloroethyl hexamethylene imine, the chlorethyl derivatives of morpholine, piperidine, pyrralidine and ethyl hexahydroaniline, di-iso-butyl-chloroethylamine and b -chloro-b 1-diethylamino-diethyl ether.ALSO:Cellulosic materials dyed with direct dyestuffs, are after-treated with polyquaternary compounds produced by contacting with water in an amount insufficient to form a homogeneous system a mono-halogenated tertiary amine of the general formula:- <FORM:0869423/IV(c)/1> wherein R1 and R2 denote similar or different hydrocarbon radicals, or R1 and R2 together with the nitrogen atom and possibly another hetero atom form a heterocyclic radical, R3 denotes a hydrocarbon radical which may contain one or more hetero-atoms and X denotes a halogen atom (see Groups IV(a) and IV(b)). The after-treatment agents may be employed in aqueous solutions, optionally together with metal compounds used for the after-treatment of direct dyeings, e.g. with copper sulphate or water soluble complex copper salts.
GB27955/57A 1956-09-08 1957-09-04 Manufacture of polyquaternary compounds Expired GB869423A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE869423X 1956-09-08

Publications (1)

Publication Number Publication Date
GB869423A true GB869423A (en) 1961-05-31

Family

ID=6802915

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27955/57A Expired GB869423A (en) 1956-09-08 1957-09-04 Manufacture of polyquaternary compounds

Country Status (1)

Country Link
GB (1) GB869423A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111138662A (en) * 2020-01-08 2020-05-12 广东德美精细化工集团股份有限公司 Preparation method and application of active hydrophilic formaldehyde-free color fixing agent
CN114479069A (en) * 2022-03-04 2022-05-13 四川大学 Novel method for directly synthesizing branched polyethyleneimine from haloethylamine

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111138662A (en) * 2020-01-08 2020-05-12 广东德美精细化工集团股份有限公司 Preparation method and application of active hydrophilic formaldehyde-free color fixing agent
CN111138662B (en) * 2020-01-08 2022-04-29 广东德美精细化工集团股份有限公司 Preparation method and application of active hydrophilic formaldehyde-free color fixing agent
CN114479069A (en) * 2022-03-04 2022-05-13 四川大学 Novel method for directly synthesizing branched polyethyleneimine from haloethylamine

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