摘要:
The present invention refers to a process for producing 5-[4-(2-hydroxy-2-methyl)-1-oxo-prop-1-yl]-3-[4-(2-hydroxy-2-methyl)-1-oxo-prop-1-yl-phenyl]-2,3-dihydro-1,1,3-trimethyl-1H-indene (dimer isomer 5) that comprises the acylation of cumene in the 4-position with an isobutyryl halide, followed by benzylic halogenation and dimerization (cyclization) of the resulting product.
摘要:
The present invention provides a Scandium catalyst that can be used in water or water-soluble organic solvent with no leaching of Scandium. Provided is a gold-polymer nanostructure-immobilized Scandium catalyst, which is formed by preparing, in liquid phase, a mixture comprising gold clusters with from 1 to 50 nm of diameter, disulfide monomer, sulfonic acid salt of disulfide and Lewis acid metal compound represented by ScY 3 , wherein Y is OSO 2 CF 3 etc., and polymerizing the mixture in the presence of a radical polymerization initiator, wherein the disulfide monomer is represented by the formula below: €ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒCH 2 =CH-R 1 -S-S-R 1 -CH=CH 2 wherein R 1 represents a divalent hydrocarbon, which may contain an ether bond, and the sulfonic acid salt of disulfide is represented by the formula below: €ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒMO 3 S-R 2 -S-S-R 2 -SO 3 M wherein R 2 represents a divalent hydrocarbon, which may contain an ether bond, and M represents an alkali metal. This catalyst is useful as a catalyst for aldol reactions, cyanolation reactions, allylation reactions, Michael reactions, Mannich reactions, Diels Alder reactions and Friedel Crafts reactions in water or water-soluble organic solvent.
摘要:
Photolabile fragrance storage substances are described, which are capable of photoinduced release of odorant aldehydes and odorant ketones. Additionally described are a process for long-lasting fragrancing of surfaces and a process for producing the fragrance storage substances mentioned.
摘要:
[PROBLEMS] To provide catalysts permitting the progress of asymmetric hydroxymethylation with high asymmetric selectivity and processes for the production of optically active hydroxymethylated compounds with the catalysts. [MEANS FOR SOLVING PROBLEMS] Use of a catalyst obtained by mixing a chiral ligand (such as compound 4) with scandium triflate or the like in the reaction of silicon enolate with formaldehyde brings about optically active hydroxymethylated compounds with high asymmetric selectivity.
摘要:
A silicon enolate represented by the following formula (Formula 1)
(in the formula, R 5 to R 7 represent hydrogen atoms, aliphatic hydrocarbon groups, monocyclic or polycyclic alicyclic hydrocarbon groups, monocyclic or polycyclic aromatic or aromatic-aliphatic hydrocarbon groups or heterocyclic groups, R 5 and R 7 are different, R 6 is not a hydrogen atom, each R 8 may be identical or different and represents a methyl group, ethyl group or isopropyl group) and formaldehyde are allowed to react in an aqueous solution or a mixed solvent of water and an organic solvent in the presence of a catalyst obtained by mixing a ligand comprising a chiral bipyridine compound or its antipode and Bi(OTf) 3 .
摘要:
A process for the preparation of an 1,1-disubstituted oxirane is disclosed, wherein an organic sulphide is reacted in a polar solvent with an educt containing a leaving group attached to a primary or secondary carbon atom, and/or the sulfonium salt formed in this way is reacted with a ketone in presence of a base and a polar solvent. Oxiranes of the type obtained may be further converted into the corresponding α-hydroxyketone or α-aminoketone, either in one step by subjecting to aerobic oxidation in the presence of a transition metal catalyst, or in two steps by hydrolyzation in the presence of an aqueous acid to the corresponding dialcohol and subsequent selective oxidation. Further described are some novel epoxide intermediates. The α-hydroxyketones and α-aminoketones thus obtainable are useful inter alia as photoinitiators.