GB653775A - Process for the manufacture of nitrogen-containing derivatives of hexoses and of compositions and baths containing the same - Google Patents

Process for the manufacture of nitrogen-containing derivatives of hexoses and of compositions and baths containing the same

Info

Publication number
GB653775A
GB653775A GB22962/48A GB2296248A GB653775A GB 653775 A GB653775 A GB 653775A GB 22962/48 A GB22962/48 A GB 22962/48A GB 2296248 A GB2296248 A GB 2296248A GB 653775 A GB653775 A GB 653775A
Authority
GB
United Kingdom
Prior art keywords
urea
hexoses
reacted
nitrogen
glucose
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
GB22962/48A
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.)
O J MEIJER S DEXTRINEFABRIEKEN
Original Assignee
O J MEIJER S DEXTRINEFABRIEKEN
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 O J MEIJER S DEXTRINEFABRIEKEN filed Critical O J MEIJER S DEXTRINEFABRIEKEN
Publication of GB653775A publication Critical patent/GB653775A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • C07H13/12Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by acids having the group -X-C(=X)-X-, or halides thereof, in which each X means nitrogen, oxygen, sulfur, selenium or tellurium, e.g. carbonic acid, carbamic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

Nitrogen-containing derivatives of hexoses are prepared by reacting hexoses (or polysaccharides which become hexoses under the reaction conditions), in the presence of a dehydrating agent with organic compounds of the general formula <FORM:0653775/IV (b)/1> in which R represents hydrogen or an alkyl, aryl or alkaryl group and X represents an oxygen or sulphur atom or the =NH group, or with melamines. Sulphuric acid, zinc chloride and phosphoric acid are suitable condensing agents. The reactants are conveniently stirred together in molten condition, preferably in the presence of not more than 20 per cent of water. In examples: (1) glucose hydrate is reacted with urea to produce a glucose ureide; (2) cane sugar is reacted with urea in the presence of some water; (3) the urea of (2) is replaced by thiourea; (4) glucose hydrate is reacted with guanidine, and (5) glucose hydrate is reacted with melamine.ALSO:Cellulosic textile materials are crease-proofed and shrink-proofed by treating them in the presence of an aldehyde with a nitrogen-containing derivative of a hexose prepared by reacting a hexose (or polysaccharide which becomes a hexose under the reaction conditions), in the presence of a dehydrating agent with a compound of the general formula <FORM:0653775/IV (c)/1> in which R is hydrogen or an alkyl, aryl or alkaryl group and X is an oxygen or sulphur atom or the =NH group. Examples are given of the reaction of glucose hydrate with urea, thiourea, guanidine or melamine, and of cane sugar with urea.
GB22962/48A 1948-01-24 1948-08-31 Process for the manufacture of nitrogen-containing derivatives of hexoses and of compositions and baths containing the same Expired GB653775A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL653775X 1948-01-24

Publications (1)

Publication Number Publication Date
GB653775A true GB653775A (en) 1951-05-23

Family

ID=19795163

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22962/48A Expired GB653775A (en) 1948-01-24 1948-08-31 Process for the manufacture of nitrogen-containing derivatives of hexoses and of compositions and baths containing the same

Country Status (1)

Country Link
GB (1) GB653775A (en)

Similar Documents

Publication Publication Date Title
US3159640A (en) Process for preparing 2-mercaptopyridine-nu oxide
Culvenor et al. 232. Reactions of ethylene oxides. Part I. Preparation of ethylene sulphides and trithiocarbonates
GB1312536A (en) Hydantoin derivatives
Hoggarth 250. Compounds related to thiosemicarbazide. Part I. 3-Phenyl-1: 2: 4-triazole derivatives
US4599425A (en) Bis-[2,5-dithio-1,3,4-thiadiazole] and a process for its production
GB653775A (en) Process for the manufacture of nitrogen-containing derivatives of hexoses and of compositions and baths containing the same
GB947634A (en) Process for the production of phosphorus compounds and their use in fire-proofing
Gregory et al. Reactions of 3-Thiocyano-2-butanone. I. The Preparation of 2-Substituted-4, 5-dimethylthiazoles
US3929877A (en) Process for the production of thiocarbohydrazide
US3265565A (en) Preparation and fungicidal use of tetracyanodithiadiene
US2853132A (en) Pest combating composition and methods employing diformamidine sulfides
US2829157A (en) Novel hydantoic acids and their alkyl esters
US4734499A (en) Preparation of α,β-diaminoacrylonitriles
US3084163A (en) Heterocyclic thioalkane sulfonic acids and methods for their production
US2375733A (en) Preparation of dithioammelide
US2402512A (en) Alpha furyl amide sulphonates
US3634513A (en) 2-methoxy-5-methyl-m-xylylenebis (isothiuronium chloride)
GB807678A (en) New substituted hydantoins and thiohydantoins
GB730923A (en) Process for the preparation of a new aldehyde derivative
NO133892B (en)
KR810000487B1 (en) Process for preparing halogen substituted benzoquanamins
US2914535A (en) 5-carbalkoxy-4-alkyl-2-thiazole-sulfenamides
Rây et al. CXCIX.—Action of monochloroacetic acid on thiocarbamide and monoalkylated thiocarbamides
GB695383A (en) An improved process for the production of xanthine and alkyl- and aryl-xanthines
GB677540A (en) Improvements in or relating to the manufacture of benziminazoles