Patent classifications
C07B43/02
Nitrosation Reagents and Methods
Provided are compounds that can find use as nitrosation reagents. Provided are nitrosation methods that include reacting a substrate with one of the provided nitrosation reagents and thereby generating a nitrosation product. Provided are kits including a nitrosation reagent. Provided are compositions wherein the nitrosation reagent is enriched in the .sup.15N isotope.
Process and plant for the adiabatic nitration of aromatic compounds
The invention relates to a method for preferably adiabatic nitration of nitratable aromatic organic compounds (aromatics) and to a corresponding plant, in particular a production plant (nitration plant) for carrying out said method.
Process and plant for the adiabatic nitration of aromatic compounds
The invention relates to a method for preferably adiabatic nitration of nitratable aromatic organic compounds (aromatics) and to a corresponding plant, in particular a production plant (nitration plant) for carrying out said method.
Method for producing C4-C15 lactams
The present invention relates to a process for preparing C.sub.4-C.sub.15 lactams, in which a C.sub.1-C.sub.10-alkyl nitrite is reacted with a C.sub.4-C.sub.15-cycloalkane and is illuminated with a light-emitting diode during the reaction. This forms a C.sub.4-C.sub.15-cyclohexanone oxime which is then converted further to a C.sub.4-C.sub.15 lactam; the C.sub.1-C.sub.10 alcohol formed is recycled into the preparation of the C.sub.1-C.sub.10-alkyl nitrite.
Method for producing C4-C15 lactams
The present invention relates to a process for preparing C.sub.4-C.sub.15 lactams, in which a C.sub.1-C.sub.10-alkyl nitrite is reacted with a C.sub.4-C.sub.15-cycloalkane and is illuminated with a light-emitting diode during the reaction. This forms a C.sub.4-C.sub.15-cyclohexanone oxime which is then converted further to a C.sub.4-C.sub.15 lactam; the C.sub.1-C.sub.10 alcohol formed is recycled into the preparation of the C.sub.1-C.sub.10-alkyl nitrite.
PROCESS AND PLANT FOR THE ADIABATIC NITRATION OF AROMATIC COMPOUNDS
The invention relates to a method for preferably adiabatic nitration of nitratable aromatic organic compounds (aromatics) and to a corresponding plant, in particular a production plant (nitration plant) for carrying out said method.
PROCESS AND PLANT FOR THE ADIABATIC NITRATION OF AROMATIC COMPOUNDS
The invention relates to a method for preferably adiabatic nitration of nitratable aromatic organic compounds (aromatics) and to a corresponding plant, in particular a production plant (nitration plant) for carrying out said method.
METHODS OF FORMING LOW SALT NITROGEN-BASED FERTILIZER
A method of forming a fertilizer can include three steps: (1) hydrolyzing a starting material to form a hydrolyzed carbon compound; (2) infusing the hydrolyzed carbon compound with nitrogen under high temperature and high pressure to form a nitrogen-infused compound; and (3) oxidizing the nitrogen-infused compound to form the fertilizer. The starting material can be a compound that has a carbon-carbon bond and/or a carbon-hydrogen bond, and in some examples the starting material is a waste or by-product, such as leftover animal feed or plastics. The fertilizer can have a low salt index.
METHODS OF FORMING LOW SALT NITROGEN-BASED FERTILIZER
A method of forming a fertilizer can include three steps: (1) hydrolyzing a starting material to form a hydrolyzed carbon compound; (2) infusing the hydrolyzed carbon compound with nitrogen under high temperature and high pressure to form a nitrogen-infused compound; and (3) oxidizing the nitrogen-infused compound to form the fertilizer. The starting material can be a compound that has a carbon-carbon bond and/or a carbon-hydrogen bond, and in some examples the starting material is a waste or by-product, such as leftover animal feed or plastics. The fertilizer can have a low salt index.
METHOD FOR PRODUCING C4-C15 LACTAMS
The present invention relates to a process for preparing C.sub.4-C.sub.15 lactams, in which a C.sub.1-C.sub.10-alkyl nitrite is reacted with a C.sub.4-C.sub.15-cycloalkane and is illuminated with a light-emitting diode during the reaction. This forms a C.sub.4-C.sub.15-cyclohexanone oxime which is then converted further to a C.sub.4-C.sub.15 lactam; the C.sub.1-C.sub.10 alcohol formed is recycled into the preparation of the C.sub.1-C.sub.10-alkyl nitrite.