GB461352A - Manufacture of condensation products and of lacquers and plastic masses therefrom - Google Patents

Manufacture of condensation products and of lacquers and plastic masses therefrom

Info

Publication number
GB461352A
GB461352A GB1985735A GB1985735A GB461352A GB 461352 A GB461352 A GB 461352A GB 1985735 A GB1985735 A GB 1985735A GB 1985735 A GB1985735 A GB 1985735A GB 461352 A GB461352 A GB 461352A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
acid
heated
ethyl
esters
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
GB1985735A
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.)
DEUTSCHEN CELLULOID FABRIK
Original Assignee
DEUTSCHEN CELLULOID FABRIK
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 DEUTSCHEN CELLULOID FABRIK filed Critical DEUTSCHEN CELLULOID FABRIK
Priority to GB1985735A priority Critical patent/GB461352A/en
Publication of GB461352A publication Critical patent/GB461352A/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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/04Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urethanes or thiourethanes
    • 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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/04Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/22Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with carboxylic acid amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paints Or Removers (AREA)

Abstract

Oily to resinous condensation products are prepared by causing an aldehyde to act upon an ester of a carbamic acid and an alcohol containing more than two carbon atoms in the presence of a compound of acid reaction. Aliphatic esters, e.g. the propyl, butyl, isobutyl, amyl, hexyl, heptyl, octyl, or isooctyl esters, hydroaromatic esters, e.g. cyclohexyl, methyl-cyclohexyl, and iso-bornyl, aralkyl, e.g. benzyl, aromatic, e.g. phenyl and cresyl, or esters of glycol mono-methyl or -ethyl ether or glycerine-acetaldehyde-acetal may be used. The carbamic acid may be substituted at the nitrogen atom by alkyl or aryl radicals, e.g. methyl, ethyl, propyl, phenyl, or cresyl. Formaldehyde or acetaldehyde or substances splitting off these aldehydes, e.g. their acetals, may be used. Acids specified are hydrochloric, phosphoric, or boric, acid salts such as zinc chloride, potassium bisulphate, or acid sodium phosphate, or organic acids, e.g. lactic, oxalic, crotonic, trichloracetic, glycollic, or mono-ethyl oxalate. The formic acid contained in commercial formaldehyde suffices, with prolonged heating. Generally, a mixture of the carbamic ester with aqueous formaldehyde is heated to dissolve the carbamic ester, the acid is added, after the ensuing spontaneous reaction the mixture is heated, the product separated and washed, and, if desired, further heated under reduced pressure. The products are soluble in alcohols, e.g. methyl, ethyl propyl, and butyl, aromatic hydrocarbons, e.g. benzene, toluene, and xylene and chlorinated hydrocarbons, and esters, e.g. methyl, ethyl, propyl, butyl, or benzyl acetate; those derived from higher aliphatic and aromatic esters dissolve in benzine and paraffin oil. They may be used for lacquers, artificial leather, and plastics, e.g. together with nitrocellulose, cellulose esters or ethers, natural or synthetic resins such as colophony, copal, dammar, shellac, condensation products of colophony with maleic anhydride or phenol-formaldehyde resins, maleic acid-colophony-glycerin condensation products, cyclohexanol resins, glycerol-phthalate or glycerol-phthalate-fatty acid resins, phenol- or alkylphenol-aldehyde resins, novolaks or resols. The oily products can replace the oil, e.g. castor oil, used in making artificial leather in conjunction with nitrocellulose &c. In examples: (1) isobutyl carbamate is dissolved, by heating, in aqueous formaldehyde, and concentrated hydrochloric acid is added. After the reaction, the mixture is refluxed, and after cooling the resin is separated, washed free from acid, and heated under reduced pressure; (2) a resin is prepared as in example (1) from cyclohexyl carbamate and formaldehyde with the aid of lactic acid; (3) a mixture of hexyl and heptyl urethanes is heated with aqueous formaldehyde, glycollic acid added when boiling, and the mixture boiled for 3 hours, the oily product is separated, washed, and heated under reduced pressure; (4) and (5) oily products are obtained as in example (3) from the carbamic ester of glycol mono-methyl ether, formaldehyde, and zinc chloride, and from the carbamic ester of glycerin-acetaldehyde acetal, formaldehyde, and mono-ethyl oxalate; (6) phenyl carbamate, aqueous formaldehyde, and hydrochloric acid are boiled under reflux to produce a resin which becomes insoluble on heating; (7) isobornyl carbamate and formaldehyde solution are heated while stirring and adding primary sodium orthophosphate, and the resulting resin heated; (8) and (9) an oil and a resin are made by adding hydrochloric acid to a heated mixture of 2-ethyl-n-hexanol and formaldehyde solution, and by adding potassium bisulphate to a heated mixture of benzyl urethane and formaldehyde solution, the mix being refluxed in both cases; (10) a condensation product from n-butyl urethane and formaldehyde prepared as in example (1) is mixed with a solvent naphtha solution of octylphenol aldehyde resin to produce a lacquer; (11) the product of example (1) is mixed with a solution of collodion cotton in butyl acetate, toluene, xylene, alcohol, and ethyl acetate, and pigmented with zinc oxide and titanium white to form a lacquer; (12) the product of example (3) is dissolved with nitrocellulose film scrap and tricresyl phosphate in alcohol and ethyl acetate and pigmented with carbon black; textile fabrics are coated with the paste to form artificial leather; (13) the product of example (4) is made with cellulose acetate and benzene-alcohol into a plastic material. The Provisional Specification describes also the production of resins from carbamic esters of polyhydric alcohols, states that the oily or resinous products are useful as adhesives for uniting cellulose derivatives or polymeric materials to one another or to metal or glass, and describes the production of an oil from n-propyl carbamate, formaldehyde, and hydrochloric acid. The oil is dissolved with collodion wool in alcohol and ethyl acetate, pigmented with zinc white and titanium white, and the paste spread on a woven fabric to provide an artificial leather, or may be used with cellulose acetate to form a plastic composition. An oil may also be produced from isobutyl carbamate and aqueous formaldehyde with the aid of phosphoric acid, and used with collodion wool to produce a plastic composition.
GB1985735A 1935-07-11 1935-07-11 Manufacture of condensation products and of lacquers and plastic masses therefrom Expired GB461352A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1985735A GB461352A (en) 1935-07-11 1935-07-11 Manufacture of condensation products and of lacquers and plastic masses therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1985735A GB461352A (en) 1935-07-11 1935-07-11 Manufacture of condensation products and of lacquers and plastic masses therefrom

Publications (1)

Publication Number Publication Date
GB461352A true GB461352A (en) 1937-02-11

Family

ID=10136356

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1985735A Expired GB461352A (en) 1935-07-11 1935-07-11 Manufacture of condensation products and of lacquers and plastic masses therefrom

Country Status (1)

Country Link
GB (1) GB461352A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2946768A (en) * 1957-08-12 1960-07-26 Bayer Ag Condensation products of carbamic acid esters
US3065232A (en) * 1962-11-20 Certificate of correction
US4162362A (en) * 1978-10-20 1979-07-24 Atlantic Richfield Company Process for the preparation of diphenylmethane dicarbamates and polymethylene polyphenyl carbamates
EP0014482A1 (en) * 1979-02-12 1980-08-20 Atlantic Richfield Company Preparation of diphenylmethane dicarbamates and polymethylene polyphenyl carbamates with Lewis acid catalysts intercalated in graphite

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065232A (en) * 1962-11-20 Certificate of correction
US2946768A (en) * 1957-08-12 1960-07-26 Bayer Ag Condensation products of carbamic acid esters
US4162362A (en) * 1978-10-20 1979-07-24 Atlantic Richfield Company Process for the preparation of diphenylmethane dicarbamates and polymethylene polyphenyl carbamates
EP0014482A1 (en) * 1979-02-12 1980-08-20 Atlantic Richfield Company Preparation of diphenylmethane dicarbamates and polymethylene polyphenyl carbamates with Lewis acid catalysts intercalated in graphite

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