PL399503A1 - Sposób otrzymywania eteru glicydylowo-1-propenylowego - Google Patents
Sposób otrzymywania eteru glicydylowo-1-propenylowegoInfo
- Publication number
- PL399503A1 PL399503A1 PL399503A PL39950312A PL399503A1 PL 399503 A1 PL399503 A1 PL 399503A1 PL 399503 A PL399503 A PL 399503A PL 39950312 A PL39950312 A PL 39950312A PL 399503 A1 PL399503 A1 PL 399503A1
- Authority
- PL
- Poland
- Prior art keywords
- pph3
- rucl2
- isomerization
- carried out
- ruh2
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 title 1
- 238000006317 isomerization reaction Methods 0.000 abstract 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 3
- DHCWLIOIJZJFJE-UHFFFAOYSA-L dichlororuthenium Chemical compound Cl[Ru]Cl DHCWLIOIJZJFJE-UHFFFAOYSA-L 0.000 abstract 3
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 abstract 2
- 150000003303 ruthenium Chemical class 0.000 abstract 2
- VYXHVRARDIDEHS-QGTKBVGQSA-N (1z,5z)-cycloocta-1,5-diene Chemical compound C\1C\C=C/CC\C=C/1 VYXHVRARDIDEHS-QGTKBVGQSA-N 0.000 abstract 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 abstract 1
- QXONIHMUSQFKJU-UHFFFAOYSA-N 2-(prop-1-enoxymethyl)oxirane Chemical compound CC=COCC1CO1 QXONIHMUSQFKJU-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052786 argon Inorganic materials 0.000 abstract 1
- 239000012300 argon atmosphere Substances 0.000 abstract 1
- PXURRFCLQDNZOY-UHFFFAOYSA-L carbon monoxide;dichlororuthenium;triphenylphosphane Chemical compound [Cl-].[Cl-].[Ru+2].[O+]#[C-].[O+]#[C-].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 PXURRFCLQDNZOY-UHFFFAOYSA-L 0.000 abstract 1
- MLIYPCQSOXNTLJ-UHFFFAOYSA-N carbon monoxide;ruthenium dihydride;triphenylphosphane Chemical compound [RuH2].[O+]#[C-].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 MLIYPCQSOXNTLJ-UHFFFAOYSA-N 0.000 abstract 1
- FMJNZRCLIZWWJP-UHFFFAOYSA-N carbon monoxide;ruthenium;triphenylphosphane Chemical compound [Ru].[O+]#[C-].[O+]#[C-].[O+]#[C-].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 FMJNZRCLIZWWJP-UHFFFAOYSA-N 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000002432 hydroperoxides Chemical class 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 239000012299 nitrogen atmosphere Substances 0.000 abstract 1
- 150000001451 organic peroxides Chemical class 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Epoxy Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Sposób otrzymywania eteru glicydylowo-1-propenylowego polega na katalitycznej bezrozpuszczalnikowej izomeryzacji eteru allilowoglicydylowego przy uzyciu jako katalizatora rozpuszczalnych kompleksów rutenu. Sposób prowadzony pod cisnieniem autogenicznym, w srodowisku beztlenowym z zastosowaniem gazu obojetnego, charakteryzuje sie tym, ze jako katalizatory reakcji stosuje sie kompleksy rutenu {[RuCl2(p-Cym)3], {[RuCl2(1,5-COD)3]x}, [RuCl2(PPh3)4], [Ru(CO)3(PPh3)2], [RuCl2(CO)2(PPh3)2], [RuHCl(CO)(AsPh3)3], [RuH2(PPh3)4], [RuH2(CO)(PPh3)3]. Reakcje izomeryzacji prowadzi sie w zakresie temperatur 80-130°C, w zakresie stezen katalizatora 0,01-1,00% mol., w czasie 1-24 godzin. Reakcji izomeryzacji poddaje sie nieczyszczony z nadtlenków i wodoronadtlenków organicznych substrat allilowy. Reakcje izomeryzacji prowadzi sie w atmosferze argonu lub azotu, przy uzyciu mieszadla magnetycznego.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL399503A PL220517B1 (pl) | 2012-06-13 | 2012-06-13 | Sposób otrzymywania eteru glicydylowo-1-propenylowego |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL399503A PL220517B1 (pl) | 2012-06-13 | 2012-06-13 | Sposób otrzymywania eteru glicydylowo-1-propenylowego |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL399503A1 true PL399503A1 (pl) | 2013-12-23 |
| PL220517B1 PL220517B1 (pl) | 2015-11-30 |
Family
ID=49767798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL399503A PL220517B1 (pl) | 2012-06-13 | 2012-06-13 | Sposób otrzymywania eteru glicydylowo-1-propenylowego |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL220517B1 (pl) |
-
2012
- 2012-06-13 PL PL399503A patent/PL220517B1/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL220517B1 (pl) | 2015-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| UA106739C2 (uk) | Спосіб одержання каталізаторів фішера-тропша та їх застосування | |
| Hargreaves | Heterogeneous catalysis with metal nitrides | |
| WO2012106349A3 (en) | High activity early transition metal carbide- and nitride-based catalysts | |
| MX2014001887A (es) | Catalizador de hidrogenacion y deshidrogenacion, y metodos para hacerlo y usarlo. | |
| HK1205048A1 (en) | Apparatus and methods for the preparation of reaction vessels with a 3d -printer | |
| IN2013MU02899A (pl) | ||
| WO2010031076A3 (en) | Conversion of prenyl derivatives to isoprene | |
| MY161105A (en) | Solid base catalyst and method for making and using the same | |
| WO2011150329A3 (en) | Carbocatalysts for chemical transformations | |
| IN2015DN02095A (pl) | ||
| BR112015009335A2 (pt) | composto de fórmula, catalisador, método para preparo dos catalisadores, e uso dos catalisadores | |
| WO2011146277A3 (en) | Methods for producing hydrocarbon products from algal biomass | |
| WO2012030065A3 (en) | Catalyst composition for hydroformylation reaction and a hydroformylation process using the same | |
| EA200901058A1 (ru) | Получение катализаторов синтеза фишера-тропша | |
| AU2013283037A8 (en) | Catalyst supports made from silicon carbide covered with TiO2 for fischer-tropsch synthesis | |
| BR112013018701A2 (pt) | catalisador de aromatização de metano, e, processos para preparar um catalisador de aromatização de metano e para produzir hidrocarbonetos aromáticos | |
| MY169719A (en) | Catalysts | |
| WO2012092512A8 (en) | Catalytic anti-markovnikov oxidation and hydration of olefins | |
| MX363925B (es) | Uso de complejos de rutenio-carbeno soportados en reactores operados cotinuamente. | |
| WO2014179648A3 (en) | Direct anti-markovnikov addition of acids to alkenes | |
| PL399503A1 (pl) | Sposób otrzymywania eteru glicydylowo-1-propenylowego | |
| Skibiński et al. | Synthesis and structure of large difluoromethylene containing alicycles by ring closing metathesis (RCM) | |
| WO2011036479A3 (en) | Process and catalyst | |
| WO2011016688A3 (ko) | 루테늄 촉매, 이의 제조방법, 및 이를 포함하는 연료전지 | |
| PL420348A1 (pl) | Sposób syntezy eterów 1-propenylowych |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LICE | Declarations of willingness to grant licence |
Free format text: RATE OF LICENCE: 10% Effective date: 20150520 |