PL410437A1 - Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it - Google Patents

Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it

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Publication number
PL410437A1
PL410437A1 PL410437A PL41043714A PL410437A1 PL 410437 A1 PL410437 A1 PL 410437A1 PL 410437 A PL410437 A PL 410437A PL 41043714 A PL41043714 A PL 41043714A PL 410437 A1 PL410437 A1 PL 410437A1
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PL
Poland
Prior art keywords
hydroxyethyl
methylammonium
alkoxymethyl
bis
obtaining
Prior art date
Application number
PL410437A
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Polish (pl)
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PL226790B1 (en
Inventor
Juliusz Pernak
Agnieszka Kurzawska
Dominika Majchrzak
Original Assignee
Politechnika Poznańska
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Application filed by Politechnika Poznańska filed Critical Politechnika Poznańska
Priority to PL410437A priority Critical patent/PL226790B1/en
Publication of PL410437A1 publication Critical patent/PL410437A1/en
Publication of PL226790B1 publication Critical patent/PL226790B1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Przedmiotem wynalazku jest salicylan alkoksymetylobis(2-hydroksyetylo)-metyloamoniowy o wzorze ogólnym 1, w którym R oznacza łańcuch węglowy zawierający od 1 do 18 atomów węgla mający zastosowanie jako środek powierzchniowo czynny oraz sposób jego otrzymywania. Sposób otrzymywania salicylanu alkoksymetylobis(2-hydroksyetylo)-metyloamoniowego polega na tym, że chlorek alkoksymetylobis(2-hydroksyetylo)-metyloamoniowy rozpuszcza się w alkoholu alifatycznym o długości łańcucha węglowego od jeden do czterech atomów węgla, lub ich mieszaninie, korzystnie w metanolu, po czym poddaje się reakcji z solą sodową lub potasową kwasu salicylowego w stosunku molowym 1:1 do 1:2, korzystnie 1:1, w temperaturze od 20 do 50°C, korzystnie 30°C, w czasie co najmniej 5 minut, a wytrąconą nieorganiczną sól odsącza się pod zmniejszonym ciśnieniem. Z kolei z otrzymanego przesączu odparowuje się rozpuszczalnik, następnie dodaje się bezwodnego acetonu w celu oczyszczenia produktu, dalej po odparowaniu acetonu pozostałość suszy się w warunkach obniżonego ciśnienia.The present invention relates to alkoxymethyl bis (2-hydroxyethyl) methylammonium salicylate of the general formula 1, wherein R is a carbon chain containing from 1 to 18 carbon atoms used as a surfactant and a method for its preparation. The method for obtaining alkoxymethylbis (2-hydroxyethyl) methylammonium salicylate is that alkoxymethylbis (2-hydroxyethyl) methylammonium chloride dissolves in an aliphatic alcohol with a carbon chain length of one to four carbon atoms, or a mixture thereof, preferably in methanol, after which is reacted with the sodium or potassium salt of salicylic acid in a molar ratio of 1: 1 to 1: 2, preferably 1: 1, at a temperature of 20 to 50 ° C, preferably 30 ° C, for at least 5 minutes, and precipitated the inorganic salt is filtered off with suction. Then the solvent is evaporated from the filtrate obtained, then anhydrous acetone is added to purify the product, and the residue is dried under reduced pressure after evaporation of the acetone.

PL410437A 2014-12-08 2014-12-08 Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it PL226790B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL410437A PL226790B1 (en) 2014-12-08 2014-12-08 Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL410437A PL226790B1 (en) 2014-12-08 2014-12-08 Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it

Publications (2)

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PL410437A1 true PL410437A1 (en) 2016-06-20
PL226790B1 PL226790B1 (en) 2017-09-29

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PL410437A PL226790B1 (en) 2014-12-08 2014-12-08 Alkoxymethyl bis(2-hydroxyethyl)methylammonium salicylate and method for obtaining it

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PL226790B1 (en) 2017-09-29

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