GB519381A - Manufacture of maltosamines - Google Patents

Manufacture of maltosamines

Info

Publication number
GB519381A
GB519381A GB27577/38A GB2757738A GB519381A GB 519381 A GB519381 A GB 519381A GB 27577/38 A GB27577/38 A GB 27577/38A GB 2757738 A GB2757738 A GB 2757738A GB 519381 A GB519381 A GB 519381A
Authority
GB
United Kingdom
Prior art keywords
maltose
methyl
hydrogen
catalyst
heated
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
GB27577/38A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB519381A publication Critical patent/GB519381A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

519,381. Maltosamines. DU PONT DE NEMOURS & CO., E. 1. Sept 21, 1938, No. 27577. Convention date, Sept. 21, 1937. [Classes 2 (iii) and 15 (ii)], Maltosamines are manufactured by the action of hydrogen in the presence of a hydrogenation catalyst on maltose and ammonia or a primary or secondary aliphatic, cycloaliphatic or araliphatic amine, or on a preformed reaction product of these compounds (which may be prepared in aqueous or alcoholic solution and appear to mostly compounds of the alcoholammonia type). The hydrogenation may be carried out below 50‹C., under elevated pressure, in the presence of a base metal catalyst, e.g. copper cobalt, copper chromite or, preferably, nickel, which may be employed in a finely divided state or supported on, porous or inert carriers such as alumina, pumice or kiesalguhr. Those of the products which contain an aliphatic radicle of at least six carbon atoms may be used as wetting, penetrating, detergent, dispersing, emulsifying, frothing and foaming agents, or, in some cases, as softening agents, whilst those which contain an aliphatic radicle of less than six carbon atoms, and maltosamine itself, yield surface-active agents on further alkylation. In examples : (1) maltose and methylamine are dissolved in water and shaken with hydrogen under pressure in the presence of a nickel catlayst to produce metbylmaltosamine; (2) maltose and dodecylamine are warmed with water and alcohol and the mixture is treated with hydrogen under pressure in the presence of a platinum oxide catalyst, yielding dedocylmaltosamine ; the product may be used as a detergent in soft, alkaline or hard water ; (3) maltose (or a dry malt containing maltose) is heated with hexadecylamine in methyl alcohol, and the resulting 1-hexadecylamino-1-hydroxymaltose is isolated and shaken with hydrogen under pressure in the presence of dioxane and a nickel catalyst or methyl alcohol and a platinum oxide catalyst, producing hexadecylmaltosamine ; the product is a softening agent for viscose rayon ; (4) maltose is heated with 9:10-octadecerylamine in methanol, and the resulting 1-octadecenylamino-1-hydroxymaltose is shaken in methanol with hydrogen under pressure in the presence of a platinum oxide catalyst, yielding octadecylmaltosamine, which is a softener for viscose rayon, and octadecenylmaltosamine, which is a detergent; (5) the hexadecylamine in (3) is-replaced by a mixture thereof with octadecylamine ; the product is a softening agent for viscose rayon; (6) a mixture of maltose, ammonia and water is shaken with hydrogen under pressure in the presence of a nickel catalyst to produce maltosamine. Other amines specified are: diethylamine, mono- and din- and isopropylamine, di-nbutylamine, monoisobutylamine, benzylamine, cyclohexylamine, naphthenylamine, aniline, N- methyl - N - isobutylamine, N - ethyl - N - hexylamine, n - octylamine, n decylamihe, N - isopropyl - N - octylamine, N - 2 - ethylhexylamine, N - methyl - N - 2 - ethylhexylamine, N - methyl - N - hexadecylamine, N - ethyl - N - tetradecylamine, undecenylamine, ricinoleylamine, oleostearylamine, the amines corresponding to the mixtures of alcohols obtained by catalytic ester hydrogenation or sodium reduction of natural fats and oils such as coconut oil, cotton seed oil, castor oil, China wood oil, sperm oil, lard oil or beef tallow or to the higher alcohols obtained in the catalytic synthesis of methanol from carbon monoxide and hydrogen, or substituted aliphatic amines, e.g. those containing aryl, ether, ester, hydroxy or sulpho groups. Maltos-amine may also be reacted with maltose to form dimaltosamine. Specifications 297,484 and 313,617, [both in Class 2 (iii)], are referred to. The Specification as open to inspection under Sect. 91 comprises also the following subject-matter: (a) The initial condensation products between maltose and ammonia or an amine may be prepared per se and employed as softening agents for viscose rayon yarn. In examples : (1) dodecylamine and maltose are heated in water to produce 1-didecylamino - 1 - hydroxymaltose ; (2) methylheptylamine and maltose are heated in methanol to yield 1 - (N - methyl - N - heptyl) - amino - 1 - hydroxymaltose; (b) maltosamine or alkylmaltosamines, e.g. methylmaltosamine, ethylmaltosamine, hydroxyethyhnaltosamine or dodecylmaltosamine, may be alkylated. In an example methylmaltosamine is heated with octadecyl bromide in the presence of sodium carbonate, benzene, ethyl and methyl alcohols and potassium iodide. The octadecyl bromide may be replaced by dodecyl chloride, dimethyl or diethyl sulphate, amyl chloride or octyl p-toluenesulphonate, the sodium carbonate by magnesium oxide, calcium carbonate, potassium carbonate, sodium acetate or 'potassium acetate, the solvent mixture by aqueous alcohol and the potassium iodide by sodium iodide ; (c) maltosamine may be reacted with an aldehyde, e.g. formaldehyde, acetaldehyde or lauraldehyde, followed or accompanied by reduction with hydrogen in the presence of a nickel catalyst ;(d) the maltosamines or the initial condensation products may be converted into salts, e.g. with hydrochloric, sulphuric, phosphoric, boric, acetic, formic, lauric, oleic or stearic acid ; (e) aniline may be used as the amine in the condensation with maltose. This subject-matter does not appear in the Specification as accepted.
GB27577/38A 1937-09-21 1938-09-21 Manufacture of maltosamines Expired GB519381A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US519381XA 1937-09-21 1937-09-21

Publications (1)

Publication Number Publication Date
GB519381A true GB519381A (en) 1940-03-26

Family

ID=21974332

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27577/38A Expired GB519381A (en) 1937-09-21 1938-09-21 Manufacture of maltosamines

Country Status (1)

Country Link
GB (1) GB519381A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2808401A (en) * 1952-11-12 1957-10-01 Gen Mills Inc Reaction products of primary fatty amines and aldose sugars
US2815339A (en) * 1952-11-26 1957-12-03 Gen Mills Inc Reaction products of primary fatty amines and ketose sugars
WO1992008687A1 (en) * 1990-11-09 1992-05-29 The Procter & Gamble Company Process for preparing n-alkyl polyhydroxy amines in amine and amine/water solvents and fatty acid amides therefrom
US5174927A (en) * 1990-09-28 1992-12-29 The Procter & Gamble Company Process for preparing brightener-containing liquid detergent compositions with polyhydroxy fatty acid amines
WO1993003004A1 (en) * 1991-07-26 1993-02-18 The Procter & Gamble Company Process for preparing n-alkyl polyhydroxyalkyl amines in aqueous/hydroxy solvents
US5194639A (en) * 1990-09-28 1993-03-16 The Procter & Gamble Company Preparation of polyhydroxy fatty acid amides in the presence of solvents
US5332528A (en) * 1990-09-28 1994-07-26 The Procter & Gamble Company Polyhydroxy fatty acid amides in soil release agent-containing detergent compositions
US5334764A (en) * 1990-10-12 1994-08-02 The Procter & Gamble Company Process for preparing N-alkyl polyhydroxy amines
US5338486A (en) * 1990-09-28 1994-08-16 The Procter & Gamble Company High catalyst process for glucamide detergents
US5338487A (en) * 1990-09-28 1994-08-16 The Procter & Gamble Company Catalyzed process for glucamide detergents
US5354425A (en) * 1993-12-13 1994-10-11 The Procter & Gamble Company Tissue paper treated with polyhydroxy fatty acid amide softener systems that are biodegradable
US5449770A (en) * 1992-01-14 1995-09-12 The Procter & Gamble Company Process for making N-alkylamino polyols
US5454982A (en) * 1990-09-28 1995-10-03 The Procter & Gamble Company Detergent composition containing polyhydroxy fatty acid amide and alkyl ester sulfonate surfactants
US5700771A (en) * 1990-09-28 1997-12-23 The Procter & Gamble Company Polyhydroxy fatty acid amide surfactants in percarbonate bleach-containing compositions
US5723673A (en) * 1995-06-07 1998-03-03 The Procter & Gamble Company Process for preparing amides of N-alkyl polyhydroxyalkyls
US5777165A (en) * 1995-06-07 1998-07-07 The Procter & Gamble Company Process for preparing amides of N-alkyl polyhydroxyalkyl amines

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2808401A (en) * 1952-11-12 1957-10-01 Gen Mills Inc Reaction products of primary fatty amines and aldose sugars
US2815339A (en) * 1952-11-26 1957-12-03 Gen Mills Inc Reaction products of primary fatty amines and ketose sugars
US5454982A (en) * 1990-09-28 1995-10-03 The Procter & Gamble Company Detergent composition containing polyhydroxy fatty acid amide and alkyl ester sulfonate surfactants
US5174927A (en) * 1990-09-28 1992-12-29 The Procter & Gamble Company Process for preparing brightener-containing liquid detergent compositions with polyhydroxy fatty acid amines
US5194639A (en) * 1990-09-28 1993-03-16 The Procter & Gamble Company Preparation of polyhydroxy fatty acid amides in the presence of solvents
US5332528A (en) * 1990-09-28 1994-07-26 The Procter & Gamble Company Polyhydroxy fatty acid amides in soil release agent-containing detergent compositions
US5338486A (en) * 1990-09-28 1994-08-16 The Procter & Gamble Company High catalyst process for glucamide detergents
US5338487A (en) * 1990-09-28 1994-08-16 The Procter & Gamble Company Catalyzed process for glucamide detergents
US5700771A (en) * 1990-09-28 1997-12-23 The Procter & Gamble Company Polyhydroxy fatty acid amide surfactants in percarbonate bleach-containing compositions
US5334764A (en) * 1990-10-12 1994-08-02 The Procter & Gamble Company Process for preparing N-alkyl polyhydroxy amines
WO1992008687A1 (en) * 1990-11-09 1992-05-29 The Procter & Gamble Company Process for preparing n-alkyl polyhydroxy amines in amine and amine/water solvents and fatty acid amides therefrom
WO1993003004A1 (en) * 1991-07-26 1993-02-18 The Procter & Gamble Company Process for preparing n-alkyl polyhydroxyalkyl amines in aqueous/hydroxy solvents
TR26107A (en) * 1991-07-26 1994-12-15 Procter & Gamble PROCESS FOR THE PREPARATION OF N-ALKYL POLYHYDROXYALKYL AMINES IN AQUEOUS/HYDROXY SOLVENT AGENTS.
US5625098A (en) * 1991-07-26 1997-04-29 The Procter & Gamble Company Process for preparing N-alkyl polyhydroxyalkyl amines in aqueous/hydroxy solvents
CN1041719C (en) * 1991-07-26 1999-01-20 普罗格特-甘布尔公司 Process for preparing N-alkyl polyhydroxyalkyl amines in aqueous/hydroxy solvents
US5449770A (en) * 1992-01-14 1995-09-12 The Procter & Gamble Company Process for making N-alkylamino polyols
US5354425A (en) * 1993-12-13 1994-10-11 The Procter & Gamble Company Tissue paper treated with polyhydroxy fatty acid amide softener systems that are biodegradable
US5723673A (en) * 1995-06-07 1998-03-03 The Procter & Gamble Company Process for preparing amides of N-alkyl polyhydroxyalkyls
US5777165A (en) * 1995-06-07 1998-07-07 The Procter & Gamble Company Process for preparing amides of N-alkyl polyhydroxyalkyl amines

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