PL421042A1 - 5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime - Google Patents

5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime

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Publication number
PL421042A1
PL421042A1 PL421042A PL42104217A PL421042A1 PL 421042 A1 PL421042 A1 PL 421042A1 PL 421042 A PL421042 A PL 421042A PL 42104217 A PL42104217 A PL 42104217A PL 421042 A1 PL421042 A1 PL 421042A1
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PL
Poland
Prior art keywords
oxime
naringenin
triethoxy
triethoxynaringenin
formula
Prior art date
Application number
PL421042A
Other languages
Polish (pl)
Other versions
PL236844B1 (en
Inventor
Joanna Kozłowska
Mirosław Anioł
Original Assignee
Uniwersytet Przyrodniczy we Wrocławiu
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Application filed by Uniwersytet Przyrodniczy we Wrocławiu filed Critical Uniwersytet Przyrodniczy we Wrocławiu
Priority to PL421042A priority Critical patent/PL236844B1/en
Publication of PL421042A1 publication Critical patent/PL421042A1/en
Publication of PL236844B1 publication Critical patent/PL236844B1/en

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

Abstract

Przedmiotem zgłoszenia jest oksym 5,7,4'-trietoksynaringeniny o wzorze 2 oraz sposób wytwarzania tego związku. Sposób ten polega na tym, że do substratu, którym jest 5,7,4'-trietoksynaringenina o wzorze 1 dodaje się chlorowodorek hydroksyloaminy oraz bezwodny octan sodu w stosunku molowym co najmniej 1:1,5:1,5 oraz minimalną ilość alkoholu, co stanowi mieszaninę reakcyjną, którą zabezpiecza się przed dostępem światła i pozostawia w temperaturze od 45°C do 55°C na okres od 10 do 24 godzin przy ciągłym mieszaniu, po czym mieszaninę wylewa się do wody z lodem, wytrącony osad sączy się pod zmniejszonym ciśnieniem, a następnie przemywa woda i osusza się.The subject of the application is 5,7,4'-triethoxynaringenin oxime of formula 2 and a method for preparing this compound. This method consists in adding hydroxylamine hydrochloride and anhydrous sodium acetate in a molar ratio of at least 1: 1.5: 1.5 and a minimum amount of alcohol to the substrate, which is 5,7,4'-triethoxynaringenin of formula 1. which is a reaction mixture, which is protected from light and left at a temperature of 45 ° C to 55 ° C for 10 to 24 hours with continuous stirring, after which the mixture is poured into ice-water, the precipitate is filtered under reduced pressure pressure, and then washed with water and dried.

PL421042A 2017-03-29 2017-03-29 5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime PL236844B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL421042A PL236844B1 (en) 2017-03-29 2017-03-29 5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL421042A PL236844B1 (en) 2017-03-29 2017-03-29 5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime

Publications (2)

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PL421042A1 true PL421042A1 (en) 2018-10-08
PL236844B1 PL236844B1 (en) 2021-02-22

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PL421042A PL236844B1 (en) 2017-03-29 2017-03-29 5,7,4'-triethoxy-naringenin-oxime and method for obtaining 5,7,4'-triethoxy naringenin-oxime

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Publication number Publication date
PL236844B1 (en) 2021-02-22

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