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DE637532C - Process for the production of silicic acid esters - Google Patents

Process for the production of silicic acid esters

Info

Publication number
DE637532C
DE637532C DEI51485D DEI0051485D DE637532C DE 637532 C DE637532 C DE 637532C DE I51485 D DEI51485 D DE I51485D DE I0051485 D DEI0051485 D DE I0051485D DE 637532 C DE637532 C DE 637532C
Authority
DE
Germany
Prior art keywords
acid esters
production
alcohol
silicic acid
orthosilicic acid
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
DEI51485D
Other languages
German (de)
Inventor
Dr Gustav Klein
Dr Hans Nienburg
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI51485D priority Critical patent/DE637532C/en
Application granted granted Critical
Publication of DE637532C publication Critical patent/DE637532C/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/04Esters of silicic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Herstellung von Kieselsäureestern Es wurde gefunden, daß man Ester der Orthokieselsäure mit Aminoalkoholen in einfacher Weise und mit guter Ausbeute herstellen kann, wenn man Orthokieselsäureester aliphatischer Alkohole, die i bis ¢ Kohlenstoffatome im Molekül enthalten, mit Monoalkylolaminen in Abwesenheit von Wasser erwärmt. Im allgemeinen arbeitet man bei Temperaturen oberhalb ioö°, zweckmäßig oberhalb i 5o'. Als Ausgangsstoffe kann man z. B. die Methyl-, Äthyl- oder Butylester der Orthokieselsäure, beispielsweise Tetraäthylorthokies-elsäureester u. dgl., verwenden. Als geeignete Monoalkylolamine seien beispielsweise Aminoäthylalkohol, Aminopropylalkohol, Aminobutylalkohol und Aminododecylalkohol genannt.Process for the production of silicic acid esters It has been found that you can esters of orthosilicic acid with amino alcohols in a simple manner and with can produce good yield if orthosilicic acid esters of aliphatic alcohols, which contain i to ¢ carbon atoms in the molecule, with monoalkylolamines in the absence heated by water. In general, one works at temperatures above ioö °, expediently above i 50 '. As starting materials you can, for. B. the methyl, ethyl or butyl esters of orthosilicic acid, for example tetraethylorthosilicic acid ester and the like. Suitable monoalkylolamines are, for example, aminoethyl alcohol, Called aminopropyl alcohol, aminobutyl alcohol and aminododecyl alcohol.

Das Verfahren kann durch einfaches Erwärmen eines Gemisches der beiden Ausgangsstoffe in Abwesenheit von Wasser vorgenommen werden. Je nachdem, ob eine vollständige oder teilweise Veresterung mit dem Monoalkylolamin erreicht werden soll, verwendet man verschiedene Mengen des Monoalkylolamins. Man kann auch in Gegenwart von nichtwässerigen Verdünnungsmitteln, z. B. von Benzol, Toluol o. dgl., arbeiten. Die Umsetzung kann unter erhöhtem Druck ausgeführt werden. Die nach dem Verfahren erhältlichen Produkte sind meist sehr leicht hydrolysierbar, wobei Kieselsäuregel ausgeschieden wird. Diese Eigenschaft macht die Orthokieselsäureester der Monoalkylolamine sehr geeignet zum Nachweis geringer Mengen Wasser in Lösungsmitteln, in denen sie sich lösen, z. B. in Alkoholen o. dgl. Weniger leicht hvdrolysierbare Monoalkylolaminortholcieselsäureester können für pharmakologische Zwecke Verwendung finden. Beispiel i i2,2 Gewichtsteile Aminoäthylalkohol werden zusammen mit io,4 Gewichsteilen Tetraäthylorthokieselsäureester 3 Stünden lang unter Ausschluß von Wasser auf i 5o° erhitzt. Der abgespaltene Alkohol wird bei ioo° im Vakuum abdestilliert, wobei der Zutritt von Feuchtigkeit vermieden wird. Das zurückbleibende farblose Öl ist der Tetra-(ß-aminoäthyl)-orthokieselsäureester. Er riecht ähnlich wie Monoäthanolamin, reagiert stark alkalisch, ist leicht löslich in wasserfreiem Methyl- und Äthylalkohol, aber unlöslich in Äther. Beim Zusammenbringen mit Äthylalkohol, der nur 2 % oder etwas weniger Wasser enthält, wird die Verbindung unter Abscheidung eines klaren Kieselsäuregels sofort hydrolysiert; - 99 °/oiger Alkohol hydrolysiert sie nach einigen Stunden. Beispiel -2 2o,8 Gewichtsteile Tetraäthyloil es> ; ';" säureester (i Mol) werden mit 3o,o'GJ ts .':' teilen i-Amino-2-propanol (4 Mol) 5x@tünden lang auf i5o° erhitzt. Der abgespaltene Alkohol und gegebenenfalls geringe Mengen' nicht umgesetzten Ausgangsstoffes werden im Vakuum bei ioo° unter Ausschluß von Feuchtigkeit abdestilliert. Das zurückbleibende dickflüssige Öl ist der Tetra-(i-amino-2-propyl)-orthokieselsäureester, der unter einem Druck von 15 mm und bei i8o° Heizbadtemperatur noch nicht destilliert. Er reagiert stark alkalisch, ist sehr leicht in Methyl-und Äthylalkohol löslich, dagegen unlöslich in er und Benzin. Durch Wasser wird der '-zlIldete Ester sofort hydrolysiert.The process can be carried out by simply heating a mixture of the two starting materials in the absence of water. Depending on whether complete or partial esterification is to be achieved with the monoalkylolamine, different amounts of the monoalkylolamine are used. You can also in the presence of non-aqueous diluents such. B. of benzene, toluene o. The like., Work. The reaction can be carried out under increased pressure. The products obtainable by the process are usually very easy to hydrolyze, with silica gel being excreted. This property makes the orthosilicic acid esters of the monoalkylolamines very suitable for the detection of small amounts of water in solvents in which they dissolve, e.g. B. in alcohols o. The like. Less easily hydrolyzable Monoalkylolaminortholcieselsäureester can be used for pharmacological purposes. EXAMPLE i 2.2 parts by weight of aminoethyl alcohol are heated to i 50 ° for 3 hours with the exclusion of water together with io.4 parts by weight of tetraethyl orthosilicic acid ester. The split off alcohol is distilled off at 100 ° in vacuo, the ingress of moisture being avoided. The remaining colorless oil is the tetra (ß-aminoethyl) orthosilicic acid ester. It smells like monoethanolamine, has a strong alkaline reaction, is easily soluble in anhydrous methyl and ethyl alcohol, but insoluble in ether. When brought into contact with ethyl alcohol, which contains only 2 % or slightly less water, the compound is immediately hydrolyzed with the separation of a clear silica gel; - 99% alcohol hydrolyzes them after a few hours. Example -2 2o.8 parts by weight of tetraethyloil es>;';" acid esters (i Mol) are with 3o, o'GJ ts. ':' share i-Amino-2-propanol (4 mol) heated to 15o ° for 5x hours. The split off alcohol and possibly small amounts of unreacted starting material are distilled off in vacuo at 100 ° with exclusion of moisture. The thick oil that remains is the tetra- (i-amino-2-propyl) orthosilicic acid ester, which has not yet distilled under a pressure of 15 mm and at a heating bath temperature of 180 °. It has a strong alkaline reaction, is very easily soluble in methyl and ethyl alcohol, but insoluble in it and petrol. The '-zlIldete is immediately hydrolyzed by water.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von Estern der Orthokieselsäure mit Monoalkylolaminen, dadurch gekennzeichnet, daß man Orthokieselsäureester aliphatischer Alkohole, die i bis q. Kohlenstoffatome im Molekül enthalten, mit Monoalkylolaminen 'in Abwesenheit von Wasser erwärmt. PATENT CLAIM: Process for the preparation of esters of orthosilicic acid with monoalkylolamines, characterized in that orthosilicic acid esters of aliphatic alcohols i to q. Carbon atoms contained in the molecule, with monoalkylolamines' heated in the absence of water.
DEI51485D 1935-01-19 1935-01-19 Process for the production of silicic acid esters Expired DE637532C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI51485D DE637532C (en) 1935-01-19 1935-01-19 Process for the production of silicic acid esters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI51485D DE637532C (en) 1935-01-19 1935-01-19 Process for the production of silicic acid esters

Publications (1)

Publication Number Publication Date
DE637532C true DE637532C (en) 1936-10-30

Family

ID=7193088

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI51485D Expired DE637532C (en) 1935-01-19 1935-01-19 Process for the production of silicic acid esters

Country Status (1)

Country Link
DE (1) DE637532C (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2885419A (en) * 1956-09-25 1959-05-05 Berkeley Chemical Corp Amino alkyl silicates
DE1125171B (en) * 1959-04-21 1962-03-08 Schering Ag Use of nitrogen-containing organic silicon compounds as curing agents for epoxy resins
US3079656A (en) * 1959-11-27 1963-03-05 Philadelphia Quartz Co Aminoalkyl polysilicates
EP0152241A3 (en) * 1984-02-04 1985-12-18 BP Chemicals Limited Transetherification process

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2885419A (en) * 1956-09-25 1959-05-05 Berkeley Chemical Corp Amino alkyl silicates
DE1125171B (en) * 1959-04-21 1962-03-08 Schering Ag Use of nitrogen-containing organic silicon compounds as curing agents for epoxy resins
US3079656A (en) * 1959-11-27 1963-03-05 Philadelphia Quartz Co Aminoalkyl polysilicates
EP0152241A3 (en) * 1984-02-04 1985-12-18 BP Chemicals Limited Transetherification process

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