PL419641A1 - Method for epoxidation of limonene - Google Patents

Method for epoxidation of limonene

Info

Publication number
PL419641A1
PL419641A1 PL419641A PL41964116A PL419641A1 PL 419641 A1 PL419641 A1 PL 419641A1 PL 419641 A PL419641 A PL 419641A PL 41964116 A PL41964116 A PL 41964116A PL 419641 A1 PL419641 A1 PL 419641A1
Authority
PL
Poland
Prior art keywords
limonene
oxidant
titanium
solvent
reaction mixture
Prior art date
Application number
PL419641A
Other languages
Polish (pl)
Other versions
PL234627B1 (en
Inventor
Agnieszka Wróblewska
Mariusz Malko
Original Assignee
Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
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 Zachodniopomorski Uniwersytet Technologiczny W Szczecinie filed Critical Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
Priority to PL419641A priority Critical patent/PL234627B1/en
Publication of PL419641A1 publication Critical patent/PL419641A1/en
Publication of PL234627B1 publication Critical patent/PL234627B1/en

Links

Landscapes

  • Epoxy Compounds (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Przedmiotem zgłoszenia jest sposób epoksydacji limonenu za pomocą 60% wodnego roztworu nadtlenku wodoru w obecności katalizatorów tytanowo-silikalitowych Ti-MCM-41 i Ti-SBA-15 oraz rozpuszczalnika, który charakteryzuje się tym, że proces prowadzi się z użyciem takich rozpuszczalników, jak toluen, acetonitryl, etanol i izopropanol, przy ich stężeniu w mieszanie reakcyjnej wynoszącym 80% wagowych, w temperaturze 0-120°C. Proces prowadzi się pod ciśnieniem atmosferycznym, przy stosunku molowym limonen/utleniacz 1:1, w czasie reakcji od 15 minut do 48 godzin, z udziałem katalizatorów tytanowo-silikalitowych w ilości 3% wag. w mieszaninie reakcyjnej, stosując intensywność mieszania 500 obr/min. Surowce wprowadza się do reaktora szklanego w następującej kolejności: limonen, rozpuszczalnik, katalizator i na końcu utleniacz.The subject of the application is a method of epoxidation of limonene with a 60% aqueous solution of hydrogen peroxide in the presence of Ti-MCM-41 and Ti-SBA-15 titanium-silica catalysts and a solvent, which is characterized by the fact that the process is carried out using solvents such as toluene , acetonitrile, ethanol and isopropanol, at a concentration in the reaction mixture of 80% by weight, at a temperature of 0-120 ° C. The process is carried out at atmospheric pressure, 1: 1 molar ratio of limonene / oxidant, during the reaction time from 15 minutes to 48 hours, with the use of titanium-silicalite catalysts in an amount of 3 wt. in the reaction mixture using a stirring intensity of 500 rpm. The raw materials are introduced into the glass reactor in the following order: limonene, solvent, catalyst and finally the oxidant.

PL419641A 2016-12-01 2016-12-01 Method for epoxidation of limonene PL234627B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL419641A PL234627B1 (en) 2016-12-01 2016-12-01 Method for epoxidation of limonene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL419641A PL234627B1 (en) 2016-12-01 2016-12-01 Method for epoxidation of limonene

Publications (2)

Publication Number Publication Date
PL419641A1 true PL419641A1 (en) 2018-06-04
PL234627B1 PL234627B1 (en) 2020-03-31

Family

ID=62223374

Family Applications (1)

Application Number Title Priority Date Filing Date
PL419641A PL234627B1 (en) 2016-12-01 2016-12-01 Method for epoxidation of limonene

Country Status (1)

Country Link
PL (1) PL234627B1 (en)

Also Published As

Publication number Publication date
PL234627B1 (en) 2020-03-31

Similar Documents

Publication Publication Date Title
EP4450129A3 (en) Nucleotide hemi-sulfate salt for the treatment of hepatitis c virus
Sakai et al. Copper (ii)-catalyzed oxidative N-nitrosation of secondary and tertiary amines with nitromethane under an oxygen atmosphere
MX2020013359A (en) PROCESS FOR PREPARING CARBONATES BY ADDITION OF CO<sub>2</sub> WITH AN EPOXIDE.
MX378594B (en) Process and intermediates for the 6,7-alpha-epoxidation of steroid 4,6-dienes
MX362989B (en) Process for the epoxidation of an olefin.
EP4570371A3 (en) Method for producing cyclic organic compound
MX381350B (en) PROCESS FOR THE PREPARATION OF 1,4-BIS (ETHOXYMETHYL) CYCLOHEXANE.
MX2021006065A (en) Processes for preparing nitrosylated propanediols, compositions comprising the same, and medical uses thereof.
CA3048084C (en) Protected oxadiazacyclic compounds, method for preparing oxadiazacyclic compounds and uses thereof
Majetich et al. Epoxidation of olefins by β-bromoalkoxydimethylsulfonium ylides
PL409652A1 (en) Method for epoxidation of limonene
PL413145A1 (en) Method for epoxidation of limonene
PL421653A1 (en) Method for oxidation of limonene
PL426054A1 (en) Method of α-Pinene oxidisation in the presence of TS-1 catalyst
BR0214173A (en) Process for reacting alkaloids, reaction product, mixture of reaction products, and use of reaction products
PL413146A1 (en) Method for epoxidation of limonene
PL423815A1 (en) Method for isomerization of limonene
SA519401887B1 (en) Process for the Production of Polyacrylonitrile
PL417821A1 (en) Method for oxidation of limonene
PL422186A1 (en) Method for oxidation of limonene to 1,2-epoxylimonene
PL423029A1 (en) Method for obtaining alpha-myrcene and alpha-pinene
PL442706A1 (en) Method of epoxidation of 1,5,9-cyclododecatriene in the liquid phase
PL423547A1 (en) Method for oxidation of limonene
PL419639A1 (en) Method for oxidation of limonene to limonene 1,2-diol and carvone
PL412605A1 (en) Method for epoxidation of limonene