Abstract:
A process for preparing 1,3-disubstituted pyrazolecarboxylic esters of the formula (I); where X, Y, Z = hydrogen or halogen and R 1 = C 1 -C 6 -alkyl, by metering an enol ether of the formula (III); where R 2 is C 1 -C 6 -alkyl at from (-41) to (-8O)°C into an alkyl hydrazine of the formula II H 2 N-NH-lower alkyl (II).
Abstract:
The present invention relates to a method for producing 2- (aminomethylidene)-4,4dihalo-3-oxobutyric acid esters of the formula (I), where R 1 , R 2 , R 3 are C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 3 -C 10 -cycloalkyl or benzyl and/or R 2 together with R 3 and the nitrogen atom, to which both radicals are bound, are a heterocyclic radical, wherein a corresponding 3-aminoacrylic acid ester is reacted with a halogen-substituted acetyl fluoride in the presence of at least one alkali or earth alkali metal fluoride. The invention also relates to the further reaction of halogen-substituted 2-(aminomethylidene)-3-oxobutyric acid esters of the formula (1) into halomethyl-substituted pyrazole-4-ylcarboxylic acids and the esters thereof.
Abstract:
The present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N-[[methyl-(1-methylethyl)amino]sulphonyl]benzamide. The invention also relates to a method for preparing this crystalline form and to formulations for crop protection which comprise this crystalline form of the phenyluracil.
Abstract:
The present invention relates to a process for manufacturing aryloxyacetamides of formula (I), by reacting haloacetamides of formula (II) with a phenol of formula (III); wherein the variables are defined according to the description, andaryloxyacetamides of formula (I).
Abstract:
The present invention relates to a method for preparing 1,3-substituted pyrazol compounds of formula (I), where X stands for a group CX 1 X 2 X 3 , with X 1 , X 2 and X 3 being hydrogen, fluorine or chlorine, independently of one another, R 1 being an C 1 -C 4 alkyl or cyclopropyl, and R 2 being hydrogen, CN or a group CO 2 R 2a , where R 2a stands for C 1 -C 6 alkyl in particular, comprising the following steps: i) reacting a compound of formula II with a hydrazone of formula (III), wherein in formula (II) the variables X and R 2 have the same meaning as indicated for formula (I), Y stands for oxygen, a group NR y1 or a group [NR y2 R y3 ] + Z - , R 3 stands for OR 3a or a group NR 3b R 3c , and wherein in formula (III) the variable R 1 has the same meaning as indicated for formula (I), R 4 and R 5 stand for hydrogen, C 1 -C 6 alkyl, alternatively substituted phenyl, independent of one another, wherein at least one of the radicals R 4 or R 5 is different from hydrogen and where R 4 and R 5 can also stand for a 5 to 10-membered saturated carbocycle together with the carbon atom connected thereto; treatment of the reaction product obtained thereby with an acid in the presence of water.