CH306565A - Process for the preparation of a mixture of p-aminobenzoic acid esters of polyethylene glycol monomethyl ethers. - Google Patents
Process for the preparation of a mixture of p-aminobenzoic acid esters of polyethylene glycol monomethyl ethers.Info
- Publication number
- CH306565A CH306565A CH306565DA CH306565A CH 306565 A CH306565 A CH 306565A CH 306565D A CH306565D A CH 306565DA CH 306565 A CH306565 A CH 306565A
- Authority
- CH
- Switzerland
- Prior art keywords
- mixture
- aminobenzoic acid
- polyethylene glycol
- glycol monomethyl
- preparation
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/612—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Gemisches von p-Aminobenzoesäureestern von Polyäthylenglykolmonomethyläthern. Es kurde die überraschende Beobachtung gemaellt, dass Ester aus p-Aminobenzoesäure und Polyäthylenglykolmonomethyläthern der Formel
EMI1.1
worin n eine ganze Zahl von 4 bis 50 bedeu tet, wertvolle therapeutische Eigenschaften aufweisen.
Das vorliegende Patent bezieht sich auf ein Verfahren zur Herstellung eines Ge misches solcher Ester, welches Verfahren da durci gekennzeichnet ist, dass man ein solehes Gemisch von Polyäthylenglykolmonomethylathern, aus welchem beim Verestern mit p-Aminobenzoesäure ein bei Temperaturen unterhalb 60 wasserlösliches Estergemisch entsteht, mit den p-Aminobenzoesäurerest abgebenden Verbindungen umsetzt ; der End- stoff hat ein wachsartiges Aussehen und ist in den meisten organischen Losungsmitteln, mit Ausnahme von aliphatischen Kohlenwasser- stoffen, leieht loslich.
Als Ausgangsstoff für das neue Verfahren geeignete Polyäthylenglykolmonomethyl ather-fiemische sind technisch leicht zugäng- lich. Die Komponenten des p-Aminobenzoe säureestergemisches weisen bezüglieh ihres Molekulargewichtes eine ähnliche Verteilung wie die Komponenten des Ausgangsproduktes auf.
Als den p-Aminobenzoylrest abgebende Verbindungen sind beispielsweise geeignet p-Aminobenzoesäure oder zum Beispiel ihre Ester mit niedrigmolekularen Alkoholen ; bei Verwendung von solchen Estern ist es zweckmässig, in der im folgenden Beispiel angegebenen Weise zu verfahren.
Das neue Estergemisch soll als Heilmittel verwendet werden.
Beispiel :
8, 25 Gewichtsteile p-Aminobenzoesäure- äthylester, 35 Gewichtsteile technischer Poly- äthylenglykolmonomethyläther vom durch- schnittlichen Molekulargewicht 350, im Hochvakuum bei 110 getrocknet, und 4 Volumteile einer 2normalen Natriummethylatlösung in Methanol werden 16 Stunden in einem Va kuum von 12 mm Quecksilber auf 100 er hitzt. Eine Probe des hellbraunen Öls ist nach dieser Zeit fast quantitativ wasserlöslich. Es wird alles auf 250 Volumteile Wasser, dem 5 Volumteile einer 2n-Salzsäure zugegeben sind, ausgegossen.
Nach Zugabe von einem Volumteil einer gesättigten Natriumbisulfitlosung wird a. uf PH 7, 5 eingestellt und mit 6 Gewichtsteilen Tierkohle während einer Stunde geschüttelt. Nach Abfiltrieren der Kohle wird das Filtrat mit Benzol mehrmals ausgeschüttelt. Alle Benzolextrakte werden dreimal mit gesättigter Natriumhydrogencar- bonatlosung gewaschen und eingedampft. Der überschüssige Polyäthylenglykol-monomethyl äther befindet sich in den wässerigen Schichten, und aus den Benzollösungen wird beim Eindampfen in Form eines hellgelben, klaren 61s das Gemiseh der p-Aminobenzoesäureester der Polyäthylenglykol-monomethyläther erhalten.
Das neue Estergemisch ist in Wasser bei Temperaturen unterhalb 510 lbslich und kann als Lokalanästhetikum verwendet werden.
Process for the preparation of a mixture of p-aminobenzoic acid esters of polyethylene glycol monomethyl ethers. The surprising observation was made that esters of p-aminobenzoic acid and polyethylene glycol monomethyl ethers of the formula
EMI1.1
where n is an integer from 4 to 50, meaning valuable therapeutic properties.
The present patent relates to a process for the preparation of a mixture of such esters, which process is characterized by the fact that a solehes mixture of polyethylene glycol monomethyl ethers, from which, when esterified with p-aminobenzoic acid, a water-soluble ester mixture is formed at temperatures below 60, with the converts p-aminobenzoic acid residue donating compounds; the end product has a waxy appearance and is slightly soluble in most organic solvents, with the exception of aliphatic hydrocarbons.
Polyethylene glycol monomethyl ether mixtures suitable as starting material for the new process are easily accessible from a technical point of view. In terms of their molecular weight, the components of the p-aminobenzoic acid ester mixture have a distribution similar to that of the components of the starting product.
Suitable compounds which donate the p-aminobenzoyl radical are, for example, p-aminobenzoic acid or, for example, its esters with low molecular weight alcohols; when using such esters it is advisable to proceed in the manner given in the following example.
The new ester mixture is said to be used as a remedy.
Example:
8, 25 parts by weight of ethyl p-aminobenzoate, 35 parts by weight of technical-grade polyethylene glycol monomethyl ether with an average molecular weight of 350, dried in a high vacuum at 110, and 4 parts by volume of a 2 normal sodium methylate solution in methanol are 16 hours in a vacuum of 12 mm of mercury to 100 he heats up. After this time, a sample of the light brown oil is almost quantitatively water-soluble. Everything is poured into 250 parts by volume of water to which 5 parts by volume of 2N hydrochloric acid have been added.
After adding one part by volume of a saturated sodium bisulfite solution, a. Adjusted to pH 7.5 and shaken with 6 parts by weight of animal charcoal for one hour. After filtering off the charcoal, the filtrate is extracted several times with benzene. All benzene extracts are washed three times with saturated sodium hydrogen carbonate solution and evaporated. The excess polyethylene glycol monomethyl ether is in the aqueous layers, and the mixture of p-aminobenzoic acid esters of polyethylene glycol monomethyl ether is obtained from the benzene solutions on evaporation in the form of a light yellow, clear 61s.
The new ester mixture is poundable in water at temperatures below 510 and can be used as a local anesthetic.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH306565T | 1950-02-15 | ||
CH298677T | 1952-12-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH306565A true CH306565A (en) | 1955-04-15 |
Family
ID=25734012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH306565D CH306565A (en) | 1950-02-15 | 1950-02-15 | Process for the preparation of a mixture of p-aminobenzoic acid esters of polyethylene glycol monomethyl ethers. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH306565A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4515981A (en) * | 1982-09-21 | 1985-05-07 | Toyo Tire & Rubber Company, Limited | Polyetherpolyol derivative and process for preparing the same |
WO1996033157A1 (en) * | 1995-04-18 | 1996-10-24 | Lambson Fine Chemicals Limited | Polyalkylene polyol esters of dialkylaminobenzoic acid and their use in photoinitiated curing processes |
-
1950
- 1950-02-15 CH CH306565D patent/CH306565A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4515981A (en) * | 1982-09-21 | 1985-05-07 | Toyo Tire & Rubber Company, Limited | Polyetherpolyol derivative and process for preparing the same |
WO1996033157A1 (en) * | 1995-04-18 | 1996-10-24 | Lambson Fine Chemicals Limited | Polyalkylene polyol esters of dialkylaminobenzoic acid and their use in photoinitiated curing processes |
US5905164A (en) * | 1995-04-18 | 1999-05-18 | Lambson Fine Chemicals Limited | Polyalkylene polyol esters of dialkylaminobenzoic acid and their use in photoinitiated curing processes |
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