ES2093963T3 - Procedimiento para la obtencion de alquilglicosidos. - Google Patents

Procedimiento para la obtencion de alquilglicosidos.

Info

Publication number
ES2093963T3
ES2093963T3 ES93908869T ES93908869T ES2093963T3 ES 2093963 T3 ES2093963 T3 ES 2093963T3 ES 93908869 T ES93908869 T ES 93908869T ES 93908869 T ES93908869 T ES 93908869T ES 2093963 T3 ES2093963 T3 ES 2093963T3
Authority
ES
Spain
Prior art keywords
weight
relation
glucose
reaction mixture
amount
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 - Lifetime
Application number
ES93908869T
Other languages
English (en)
Inventor
Gerhard Wolf
Alfred Oftring
Georg Schuh
Helmut Wolf
Rudolf Alt
Hans-Heinrich Bechtolsheimer
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of ES2093963T3 publication Critical patent/ES2093963T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime 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

Landscapes

  • 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)
  • Saccharide Compounds (AREA)
  • Detergent Compositions (AREA)

Abstract

ELABORACION DE GLICOSIDOS ALQUIL MEDIANTE LA CONVERSION DE GLICOSAS ACUOSAS CON AGUA, CONTENIENDO DESDE 10 HASTA 80 % EN PESO DE ALCOHOLES PRIMARIOS ALIFATICOS CON 5 HASTA 30 ATOMOS DE C EN DONDE: (A) LOS ALCOHOLES Y LAS GLICOSAS SON UTILIZADAS EN RELACION MOLAR DE 2:1 HASTA 10:1; (B) 0,1 HASTA 5 % EN PESO DE ACIDO A PARTIR DE UN SURFACTANTE ANIONICO EN RELACION A LA CANTIDAD DE GLUCOSAS EN UN CATALIZADOR ACIDO CON PROPIEDADES DE EMULSIFICACION; (C) 1 HASTA 30 % EN PESO DE ALQUIL GLICOSIDOS EN RELACION A LA CANTIDAD DE GLICOSAS UTILIZADAS, QUE SON EMPLEADOS COMO UN EMULSIFICADOR POSTERIOR; (D) LA GLUCOSA ACUOSA ES CALENTADA PREVIAMENTE DESDE 50 HASTA 90 SA PRECALENTADA DE GLUCOSA SE DOSIFICA CORRECTAMENTE Y SE MEZCLA PARA PRODUCIR UN ALCOHOL DE MEZCLA DE REACCION, CATALIZADOR ACIDO Y EMULSIFICADOR DE TAL MODO QUE SE PRODUCE UNA EMULSION; (E) LA CONVERSION TIENE LUGAR EN UNA TEMPERATURA DESDE 100 HASTA 150 AÑADIDO A LA MEZCLA DE REACCION Y PRODUCIDA MEDIANTE CONVERSION SE DESTILA DE FORMA CONTINUA; (F) DESPUES DE QUE LA REACCION HA SIDO DIRIGIDA DE FORMA SATISFACTORIA, EL CATALIZADOR ACIDO ES NEUTRALIZADO MEDIANTE LA ADICION DE UNA BASE DE FORMA QUE LA MEZCLA RESULTANTE DISPONE DE UN PH DESDE 8 HASTA 10; DE DONDE (G) EL ALCOHOL EN EXCESO SE DESTILA A UNA PRESION DESDE 0,01 HASTA 10 MBAR MIENTRAS QUE EL CONTENIDO RESIDUAL ES MENOR DEL 5 % EN RELACION A LA CANTIDAD DE GLUCOSIDO ALQUIL, Y (H) LA MEZCLA DE REACCION ES BLANQUEADA CON UN COMPUESTO DE SEPARACION DE OXIGENO ACTIVO DESPUES DE QUE HA SIDO CONVERTIDA EN UNA PASTA ACUOSA CON 30 HASTA 70 % EN PESO DE GLUCOSIDO ALQUIL CON UN PH DESDE 8 HASTA 10.
ES93908869T 1992-04-10 1993-04-01 Procedimiento para la obtencion de alquilglicosidos. Expired - Lifetime ES2093963T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4212080A DE4212080A1 (de) 1992-04-10 1992-04-10 Verfahren zur Herstellung von Alkylglykosiden

Publications (1)

Publication Number Publication Date
ES2093963T3 true ES2093963T3 (es) 1997-01-01

Family

ID=6456548

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93908869T Expired - Lifetime ES2093963T3 (es) 1992-04-10 1993-04-01 Procedimiento para la obtencion de alquilglicosidos.

Country Status (7)

Country Link
US (1) US5554742A (es)
EP (1) EP0635022B1 (es)
JP (1) JP3511060B2 (es)
CA (1) CA2124071A1 (es)
DE (2) DE4212080A1 (es)
ES (1) ES2093963T3 (es)
WO (1) WO1993021196A1 (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4316601A1 (de) * 1993-05-18 1994-11-24 Henkel Kgaa Verfahren zur Herstellung hellfarbiger Alkyl- und/oder Alkenyloligoglycoside
DE4423641C1 (de) * 1994-07-06 1995-09-07 Henkel Kgaa Verfahren zur Herstellung hellfarbiger Tenside
FR2723858B1 (fr) 1994-08-30 1997-01-10 Ard Sa Procede de preparation d'agents tensioactifs a partir de sous-produits du ble et nouveaux xylosides d'alkyle
DE4432689A1 (de) * 1994-09-14 1996-03-21 Basf Ag Mischung aus Alkylierungsprodukten von acetalisierten Monosacchariden mit Epoxiden
US6555515B1 (en) * 1995-12-06 2003-04-29 Henkel Kommanitgesellschaft Auf Aktien Formulations for cleaning hard surfaces based on at least partly branched-chain alkyl oligoglucosides
DE19546416A1 (de) 1995-12-12 1997-06-19 Basf Ag Ölemulsion
US6060636A (en) 1996-09-04 2000-05-09 Kimberly-Clark Worldwide, Inc. Treatment of materials to improve handling of viscoelastic fluids
US6204369B1 (en) * 1999-06-08 2001-03-20 Henkel Corporation Process for the preparation of alykl polyglycosides
CA2409136A1 (en) * 2000-05-18 2001-11-22 The Lubrizol Corporation Process for reacting large hydrophobic molecules with small hydrophilic molecules
ATE363827T1 (de) * 2001-04-12 2007-06-15 Basf Ag Bioregulatorische wirkstoffkombination
ATE358421T1 (de) * 2002-08-19 2007-04-15 Basf Ag Carbonsäure-haltige mittel und deren verwendung im pflanzenanbau
JP4732174B2 (ja) * 2005-01-31 2011-07-27 独立行政法人科学技術振興機構 グリコシド化合物の製造方法
JP2014125474A (ja) * 2012-12-27 2014-07-07 Kao Corp アルキルグリコシドの製造方法
KR101488862B1 (ko) * 2014-07-11 2015-02-06 주식회사 그린켐텍 고급 알킬폴리글리코시드의 제조방법
CN114920687B (zh) * 2022-05-25 2024-04-09 南京红太阳生物化学有限责任公司 一种4,4′-联吡啶的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0096917A1 (en) * 1982-06-14 1983-12-28 THE PROCTER & GAMBLE COMPANY Process for preparation of alkyl glycosides
EP0132043B2 (en) * 1983-06-15 1994-08-31 THE PROCTER & GAMBLE COMPANY Improved process for preparing alkyl glycosides
US4721780A (en) * 1985-02-06 1988-01-26 A. E. Staley Manufacturing Company Glycoside preparation directly from aqueous saccharide solutions or syrups
DE3623246A1 (de) * 1986-07-10 1988-01-14 Huels Chemische Werke Ag Verfahren zur herstellung von butyloligoglycosiden
US4996306A (en) * 1988-04-05 1991-02-26 Henkel Kommanditgesellschaft Auf Aktien Glycoside preparation directly from aqueous saccharide solutions or syrups
DE3833780A1 (de) * 1988-10-05 1990-04-12 Henkel Kgaa Verfahren zur direkten herstellung von alkylglykosiden
US5003057A (en) * 1988-12-23 1991-03-26 Henkel Kommanditgesellschaft Auf Aktien Process for production of glycosides
DE3927919C2 (de) * 1989-08-24 2002-10-31 Cognis Deutschland Gmbh Verfahren zur Herstellung von Alkylglykosiden

Also Published As

Publication number Publication date
CA2124071A1 (en) 1993-10-28
JP3511060B2 (ja) 2004-03-29
JPH07505403A (ja) 1995-06-15
EP0635022B1 (de) 1996-11-06
DE59304432D1 (de) 1996-12-12
DE4212080A1 (de) 1993-10-14
US5554742A (en) 1996-09-10
WO1993021196A1 (de) 1993-10-28
EP0635022A1 (de) 1995-01-25

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