Patent classifications
C07C41/26
Monocarbonyl ruthenium and osmium catalysts
The invention relates to monocarbonyl complexes of ruthenium and osmium with bi- and tridentate nitrogen and phosphine ligands. The invention relates to methods for preparing these complexes and the use of these complexes, isolated or prepared in situ, as catalysts for reduction reactions of ketones and aldehydes both via transfer hydrogenation or hydrogenation with hydrogen.
MODIFIED ORGANOMETALLIC FRAMEWORK AND CATALYST FOR HYDROGENATION REACTION INCLUDING SAME
The present disclosure relates to an organometallic framework modified using a compound having a hydroxyl group (—OH), a catalyst for a hydrogenation reaction including the same, and a method of manufacturing the same. The catalyst according to the present disclosure has high activity to the hydrogenation reaction even at a low temperature of 30 to 40° C., thus making low-grade waste heat usable.
MODIFIED ORGANOMETALLIC FRAMEWORK AND CATALYST FOR HYDROGENATION REACTION INCLUDING SAME
The present disclosure relates to an organometallic framework modified using a compound having a hydroxyl group (—OH), a catalyst for a hydrogenation reaction including the same, and a method of manufacturing the same. The catalyst according to the present disclosure has high activity to the hydrogenation reaction even at a low temperature of 30 to 40° C., thus making low-grade waste heat usable.
Dialkoxyalkadienyne compound and a process for preparing the same and a process for preparing a dienynal compound
A process for preparing a dienynal compound of the following general formula (2):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCHO (2), wherein n represents an integer of 0 to 11, the process comprising a step of hydrolyzing a dialkoxyalkadienyne compound of the following general formula (1):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCH(OR.sup.1)(OR.sup.2) (1) wherein R.sup.1 and R.sup.2 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, preferably 1 to 8, more preferably 1 to 4, or R.sup.1 and R.sup.2 may be bonded to each other to form a divalent hydrocarbon group, R.sup.1-R.sup.2, having from 2 to 10 carbon atoms, and n represents an integer of 0 to 11, to obtain the dienynal compound (2). ##STR00001##
Dialkoxyalkadienyne compound and a process for preparing the same and a process for preparing a dienynal compound
A process for preparing a dienynal compound of the following general formula (2):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCHO (2), wherein n represents an integer of 0 to 11, the process comprising a step of hydrolyzing a dialkoxyalkadienyne compound of the following general formula (1):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCH(OR.sup.1)(OR.sup.2) (1) wherein R.sup.1 and R.sup.2 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, preferably 1 to 8, more preferably 1 to 4, or R.sup.1 and R.sup.2 may be bonded to each other to form a divalent hydrocarbon group, R.sup.1-R.sup.2, having from 2 to 10 carbon atoms, and n represents an integer of 0 to 11, to obtain the dienynal compound (2). ##STR00001##
DEGRADABLE POLYMERS AND MONOMERS THEREFOR
Hydroxyacetal or hydroxyketal monomers, processes for their preparation, their use to produce degradable polymers, hydroxy-functional intermediates resulting from degradation, and repurposed polymers made from the hydroxy-functional intermediates are described. The invention avoids the energy-intensive conditions normally used to degrade polyurethanes and generates new hydroxy-functional intermediates that can be repurposed or upcycled. Polyurethanes and melamines, materials once destined for a landfill, can have a second life. Incorporation of a photoacid generator into microcapsule core materials and fabrication of the shell from the hydroxy-functional acetal or ketal monomers promotes facile, inside-out, solid-state degradation of the microcapsule shell triggered by UV light and acid generation in a hydrophobic environment. This enables controlled release of flavors, fragrances, biocides, agricultural actives, or other oil-based beneficial agents from within the microcapsules.
Process for the preparation of treprostinil
Treprostinil is a synthetic prostacyclin derivative with thrombocyte aggregation inhibitory and vasodilatory activity. Treprostinil can be administered in subcutaneous, intravenous, inhalable, or oral forms. Disclosed is a method for the preparation of treprostinil of formula I and its amorphous form, anhydrate form, monohydrate form, and polyhydrate form salts with bases. In the disclosed method, the chiral center in the 3-hydroxyoctyl substituent is formed at the end of the synthesis, so that the method is robust and well scalable. Also disclosed are treprostinil intermediates and the preparation of the intermediates. ##STR00001##
Process for the preparation of treprostinil
Treprostinil is a synthetic prostacyclin derivative with thrombocyte aggregation inhibitory and vasodilatory activity. Treprostinil can be administered in subcutaneous, intravenous, inhalable, or oral forms. Disclosed is a method for the preparation of treprostinil of formula I and its amorphous form, anhydrate form, monohydrate form, and polyhydrate form salts with bases. In the disclosed method, the chiral center in the 3-hydroxyoctyl substituent is formed at the end of the synthesis, so that the method is robust and well scalable. Also disclosed are treprostinil intermediates and the preparation of the intermediates. ##STR00001##
METHOD FOR DEPOLYMERISING OXYGENATED POLYMER MATERIALS BY NUCLEOPHILIC CATALYSIS
The present invention relates to a method for depolymerising oxygenated polymer materials, in particular by nucleophilic catalysis and to the use of said method in the recycling of plastic materials and the preparation of aromatic and aliphatic compounds that can be used as fuel, synthesis intermediates, raw materials in the construction sector, and in the petrochemical, electrical, electronic, textile, aeronautical, pharmaceutical, cosmetic and agrochemical industry. The present invention also relates to a method for manufacturing fuels, electronic components, plastic polymers, rubber, medicines, vitamins, cosmetics, perfumes, food products, synthetic yarns and fibres, synthetic leathers, glues, pesticides, fertilisers comprising (i) a step of depolymerisation of oxygenated polymer materials according to the method of the invention and optionally (ii) a step of hydrolysis, and optionally (iii) a step of functionalisation and/or defunctionalisation.
METHOD FOR DEPOLYMERISING OXYGENATED POLYMER MATERIALS BY NUCLEOPHILIC CATALYSIS
The present invention relates to a method for depolymerising oxygenated polymer materials, in particular by nucleophilic catalysis and to the use of said method in the recycling of plastic materials and the preparation of aromatic and aliphatic compounds that can be used as fuel, synthesis intermediates, raw materials in the construction sector, and in the petrochemical, electrical, electronic, textile, aeronautical, pharmaceutical, cosmetic and agrochemical industry. The present invention also relates to a method for manufacturing fuels, electronic components, plastic polymers, rubber, medicines, vitamins, cosmetics, perfumes, food products, synthetic yarns and fibres, synthetic leathers, glues, pesticides, fertilisers comprising (i) a step of depolymerisation of oxygenated polymer materials according to the method of the invention and optionally (ii) a step of hydrolysis, and optionally (iii) a step of functionalisation and/or defunctionalisation.