Abstract:
A process for the preparation of a zeolitic material having a structure comprising YO 2 and X 2 O 3 is provided, wherein said process comprises the steps of ( 1 ) providing a mixture comprising one or more ammonium compounds of which the ammonium cation has the formula (I): [R 1 R 2 NR 3 R 4+ (I) and further comprising one or more sources for Y0 2 and one or more sources for X 2 O 3 ; (2) crystallizing the mixture provided in step ( 1 ); wherein Y is a tetravalent element, and X is a trivalent element, and wherein the ammonium compounds are preferably derivatized or underivatized N,N-dimethylpyrrolidinium compounds, Ν,Ν-dimethylpiperidinium compounds, Ν,Ν-dimethylhexahydroazepinium compounds, and mixtures thereof, and wherein the molar ratio of ammonium cation having the formula (I) to Y in the mixture provided in step (1) and crystallized in step (2) is equal to or greater than 0.25.
Abstract:
The present invention relates to a process for preparing,4-bis(ethoxymethyl)cyclohexane, which comprises reacting1,4-bis(hydroxymethyl)cyclohexane with ethyl chloride in the presence of an inorganic base, a solvent and a phase transfer catalyst to yield a reaction mixture containing 1,4-bis(ethoxymethyl)cyclohexane, where the inorganic base is selected from alkali metal hydroxides and earth alkaline metal hydroxides and where the solvent is selected from water or a mixture of water with at least one organic solvent.
Abstract:
The present invention relates to acetylene bridged linkers, metal-organic frameworks produced thereof, processes for producing the linkers and the MOFs and their use.
Abstract:
The present invention relates to a method for preparing a compound of formula (I). The present invention also relates to compounds of formula (A) or a compound in the form of a stereoisomer. The present invention further relates to the use of a compound of formula (A) as aroma chemical.
Abstract:
The present invention relates to a process for preparing 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-en-1-one, which comprises a) providing 6,10-dimethylundeca-1,5,9-trien-4-ol, b) oxidizing 6,10-dimethylundeca-1,5,9-trien-4-ol provided in step a) with an oxidizing agent in the presence of at least one organic nitroxyl radical, at least one nitrate compound and an inorganic solid to yield 6,10-dimethylundeca-1,5,9-trien-4-one, c) reacting the 6,10-dimethylundeca-1,5,9-trien-4-one obtained in step b) with an acid to yield 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-en-1-one.